NO970685L - Festeanordning for et sanitærelement - Google Patents

Festeanordning for et sanitærelement

Info

Publication number: NO970685L
Authority: NO; Norway
Prior art keywords: butyl; imidazol; phenoxy; chloride; hours
Prior art date: 1996-02-16

Application number

NO970685A

Other languages

English (en)

Norwegian (no)

Other versions

NO970685D0 (no

Inventor

Adolf Schweigert

Gregor Krzempek

Original Assignee

Friatec Keramik Kunststoff

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1996-02-16

Filing date

1997-02-14

Publication date

1997-08-18

1997-02-14 Application filed by Friatec Keramik Kunststoff filed Critical Friatec Keramik Kunststoff

1997-02-14 Publication of NO970685D0 publication Critical patent/NO970685D0/no

1997-08-18 Publication of NO970685L publication Critical patent/NO970685L/no

Links

XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 86
238000000034 method Methods 0.000 claims description 49
239000004033 plastic Substances 0.000 claims description 6
229920003023 plastic Polymers 0.000 claims description 6
238000004519 manufacturing process Methods 0.000 claims description 5
239000000969 carrier Substances 0.000 claims description 3
229910052751 metal Inorganic materials 0.000 claims description 2
239000002184 metal Substances 0.000 claims description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 220
150000001875 compounds Chemical class 0.000 claims 137
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 111
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 99
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 77
235000019441 ethanol Nutrition 0.000 claims 74
239000007787 solid Substances 0.000 claims 67
239000000243 solution Substances 0.000 claims 61
239000000203 mixture Substances 0.000 claims 60
239000002244 precipitate Substances 0.000 claims 53
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 45
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims 42
238000010992 reflux Methods 0.000 claims 39
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 36
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims 30
239000011541 reaction mixture Substances 0.000 claims 30
238000001953 recrystallisation Methods 0.000 claims 30
-1 phenylthio, phenylsulfinyl Chemical group 0.000 claims 29
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 28
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 28
239000000047 product Substances 0.000 claims 25
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 24
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 21
239000000706 filtrate Substances 0.000 claims 21
239000002904 solvent Substances 0.000 claims 21
KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims 19
125000000217 alkyl group Chemical group 0.000 claims 19
229910052760 oxygen Inorganic materials 0.000 claims 17
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 17
239000000725 suspension Substances 0.000 claims 17
238000006243 chemical reaction Methods 0.000 claims 16
150000003839 salts Chemical class 0.000 claims 16
238000003756 stirring Methods 0.000 claims 16
238000002360 preparation method Methods 0.000 claims 15
230000036982 action potential Effects 0.000 claims 14
238000001816 cooling Methods 0.000 claims 14
239000003921 oil Substances 0.000 claims 14
235000019198 oils Nutrition 0.000 claims 14
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 14
QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 claims 12
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims 12
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 11
238000009835 boiling Methods 0.000 claims 11
239000001301 oxygen Substances 0.000 claims 11
SFONMQPCERJOJE-UHFFFAOYSA-N 4-(4-imidazol-1-ylphenoxy)butan-1-amine;dihydrochloride Chemical compound Cl.Cl.C1=CC(OCCCCN)=CC=C1N1C=NC=C1 SFONMQPCERJOJE-UHFFFAOYSA-N 0.000 claims 10
239000003416 antiarrhythmic agent Substances 0.000 claims 10
230000015572 biosynthetic process Effects 0.000 claims 10
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 9
239000013078 crystal Substances 0.000 claims 9
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims 8
238000001914 filtration Methods 0.000 claims 8
239000002585 base Substances 0.000 claims 7
239000011734 sodium Substances 0.000 claims 7
JQDUSOHGIHANJS-UHFFFAOYSA-N 2-[4-(4-acetylphenoxy)butyl]isoindole-1,3-dione Chemical compound C1=CC(C(=O)C)=CC=C1OCCCCN1C(=O)C2=CC=CC=C2C1=O JQDUSOHGIHANJS-UHFFFAOYSA-N 0.000 claims 6
RKIDDEGICSMIJA-UHFFFAOYSA-N 4-chlorobenzoyl chloride Chemical compound ClC(=O)C1=CC=C(Cl)C=C1 RKIDDEGICSMIJA-UHFFFAOYSA-N 0.000 claims 6
YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 claims 6
QRIZORZKXLSBRO-UHFFFAOYSA-N 5-(4-imidazol-1-ylphenoxy)pentan-1-amine Chemical compound C1=CC(OCCCCCN)=CC=C1N1C=NC=C1 QRIZORZKXLSBRO-UHFFFAOYSA-N 0.000 claims 6
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 6
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 6
JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 claims 6
PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 claims 6
150000001412 amines Chemical class 0.000 claims 6
230000003288 anthiarrhythmic effect Effects 0.000 claims 6
238000001035 drying Methods 0.000 claims 6
229910052739 hydrogen Inorganic materials 0.000 claims 6
239000000543 intermediate Substances 0.000 claims 6
239000007788 liquid Substances 0.000 claims 6
238000004949 mass spectrometry Methods 0.000 claims 6
125000001424 substituent group Chemical group 0.000 claims 6
238000003786 synthesis reaction Methods 0.000 claims 6
ADGHNIFLKSLROX-UHFFFAOYSA-N 4-[4-(tetrazol-1-yl)phenoxy]butan-1-amine;hydrochloride Chemical compound Cl.C1=CC(OCCCCN)=CC=C1N1N=NN=C1 ADGHNIFLKSLROX-UHFFFAOYSA-N 0.000 claims 5
OOOGOCOFYSFFOK-UHFFFAOYSA-N 4-methyl-n-[4-(4-nitrophenoxy)butyl]benzenesulfonamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NCCCCOC1=CC=C([N+]([O-])=O)C=C1 OOOGOCOFYSFFOK-UHFFFAOYSA-N 0.000 claims 5
BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 claims 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 5
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 5
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims 5
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims 5
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims 5
229910052757 nitrogen Inorganic materials 0.000 claims 5
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 5
229910000104 sodium hydride Inorganic materials 0.000 claims 5
229940124530 sulfonamide Drugs 0.000 claims 5
229910052717 sulfur Inorganic materials 0.000 claims 5
DRLZMMIQNNWJQC-UHFFFAOYSA-N 2-[4-(4-nitrophenoxy)butyl]isoindole-1,3-dione Chemical compound C1=CC([N+](=O)[O-])=CC=C1OCCCCN1C(=O)C2=CC=CC=C2C1=O DRLZMMIQNNWJQC-UHFFFAOYSA-N 0.000 claims 4
KLMVSQKATLRFGL-UHFFFAOYSA-N 4-(4-imidazol-1-ylphenoxy)butan-1-amine Chemical compound C1=CC(OCCCCN)=CC=C1N1C=NC=C1 KLMVSQKATLRFGL-UHFFFAOYSA-N 0.000 claims 4
KMMHZIBWCXYAAH-UHFFFAOYSA-N 4-bromobenzenesulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=C(Br)C=C1 KMMHZIBWCXYAAH-UHFFFAOYSA-N 0.000 claims 4
DENKGPBHLYFNGK-UHFFFAOYSA-N 4-bromobenzoyl chloride Chemical compound ClC(=O)C1=CC=C(Br)C=C1 DENKGPBHLYFNGK-UHFFFAOYSA-N 0.000 claims 4
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims 4
KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 4
ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 claims 4
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims 4
239000002253 acid Substances 0.000 claims 4
229910052804 chromium Inorganic materials 0.000 claims 4
238000010790 dilution Methods 0.000 claims 4
239000012895 dilution Substances 0.000 claims 4
239000010410 layer Substances 0.000 claims 4
230000000144 pharmacologic effect Effects 0.000 claims 4
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims 4
239000012312 sodium hydride Substances 0.000 claims 4
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 claims 4
238000005406 washing Methods 0.000 claims 4
UXFWTIGUWHJKDD-UHFFFAOYSA-N 2-(4-bromobutyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCCCBr)C(=O)C2=C1 UXFWTIGUWHJKDD-UHFFFAOYSA-N 0.000 claims 3
SSOQEARLTIELAX-UHFFFAOYSA-N 2-[3-(4-aminophenoxy)propyl]isoindole-1,3-dione;hydrochloride Chemical compound Cl.C1=CC(N)=CC=C1OCCCN1C(=O)C2=CC=CC=C2C1=O SSOQEARLTIELAX-UHFFFAOYSA-N 0.000 claims 3
JHMWPJKKCXHSPK-UHFFFAOYSA-N 2-[3-(4-imidazol-1-ylphenoxy)propyl]isoindole-1,3-dione Chemical compound O=C1C2=CC=CC=C2C(=O)N1CCCOC(C=C1)=CC=C1N1C=CN=C1 JHMWPJKKCXHSPK-UHFFFAOYSA-N 0.000 claims 3
IXFMYAHRGLUFFD-UHFFFAOYSA-N 2-[4-(4-benzoylphenoxy)butyl]isoindole-1,3-dione Chemical compound C=1C=C(OCCCCN2C(C3=CC=CC=C3C2=O)=O)C=CC=1C(=O)C1=CC=CC=C1 IXFMYAHRGLUFFD-UHFFFAOYSA-N 0.000 claims 3
VJRJMTIFYQLUOE-UHFFFAOYSA-N 4-(4-imidazol-1-ylphenoxy)butan-1-amine;hydrochloride Chemical compound Cl.C1=CC(OCCCCN)=CC=C1N1C=NC=C1 VJRJMTIFYQLUOE-UHFFFAOYSA-N 0.000 claims 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 3
UHEGNGLULAKXMN-UHFFFAOYSA-N Cl.C1=CC(OCCCCN)=CC=C1C1=CC=NC=N1 Chemical compound Cl.C1=CC(OCCCCN)=CC=C1C1=CC=NC=N1 UHEGNGLULAKXMN-UHFFFAOYSA-N 0.000 claims 3
RIMIIZIAJAFZNJ-UHFFFAOYSA-N Cl.C1=CC(OCCCCN)=CC=C1C1=NNC=C1 Chemical compound Cl.C1=CC(OCCCCN)=CC=C1C1=NNC=C1 RIMIIZIAJAFZNJ-UHFFFAOYSA-N 0.000 claims 3
239000007995 HEPES buffer Substances 0.000 claims 3
239000012359 Methanesulfonyl chloride Substances 0.000 claims 3
ZSXGLVDWWRXATF-UHFFFAOYSA-N N,N-dimethylformamide dimethyl acetal Chemical compound COC(OC)N(C)C ZSXGLVDWWRXATF-UHFFFAOYSA-N 0.000 claims 3
102000004257 Potassium Channel Human genes 0.000 claims 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 3
239000004480 active ingredient Substances 0.000 claims 3
MXMOTZIXVICDSD-UHFFFAOYSA-N anisoyl chloride Chemical compound COC1=CC=C(C(Cl)=O)C=C1 MXMOTZIXVICDSD-UHFFFAOYSA-N 0.000 claims 3
125000003118 aryl group Chemical group 0.000 claims 3
230000000903 blocking effect Effects 0.000 claims 3
239000003795 chemical substances by application Substances 0.000 claims 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims 3
239000006185 dispersion Substances 0.000 claims 3
229940079593 drug Drugs 0.000 claims 3
239000003814 drug Substances 0.000 claims 3
239000003937 drug carrier Substances 0.000 claims 3
230000000694 effects Effects 0.000 claims 3
239000012458 free base Substances 0.000 claims 3
238000002844 melting Methods 0.000 claims 3
QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 claims 3
XCOBRBQJQGKQHY-UHFFFAOYSA-N n-[4-(4-aminophenoxy)butyl]-4-methylbenzenesulfonamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NCCCCOC1=CC=C(N)C=C1 XCOBRBQJQGKQHY-UHFFFAOYSA-N 0.000 claims 3
YICWCAXQBGBRDJ-UHFFFAOYSA-N n-[4-(4-cyanophenoxy)butyl]-4-methylbenzenesulfonamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NCCCCOC1=CC=C(C#N)C=C1 YICWCAXQBGBRDJ-UHFFFAOYSA-N 0.000 claims 3
210000003540 papillary muscle Anatomy 0.000 claims 3
229920001223 polyethylene glycol Polymers 0.000 claims 3
108020001213 potassium channel Proteins 0.000 claims 3
238000000746 purification Methods 0.000 claims 3
230000002336 repolarization Effects 0.000 claims 3
229910052938 sodium sulfate Inorganic materials 0.000 claims 3
235000011152 sodium sulphate Nutrition 0.000 claims 3
ZBMZVLHSJCTVON-UHFFFAOYSA-N sotalol Chemical compound CC(C)NCC(O)C1=CC=C(NS(C)(=O)=O)C=C1 ZBMZVLHSJCTVON-UHFFFAOYSA-N 0.000 claims 3
229960002370 sotalol Drugs 0.000 claims 3
239000006228 supernatant Substances 0.000 claims 3
230000001225 therapeutic effect Effects 0.000 claims 3
NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 claims 2
GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims 2
CXAICGCTHOWKPP-UHFFFAOYSA-N 2,1,3-benzothiadiazole-4-sulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CC2=NSN=C12 CXAICGCTHOWKPP-UHFFFAOYSA-N 0.000 claims 2
OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 claims 2
GFISDBXSWQMOND-UHFFFAOYSA-N 2,5-dimethoxyoxolane Chemical compound COC1CCC(OC)O1 GFISDBXSWQMOND-UHFFFAOYSA-N 0.000 claims 2
VKJCJJYNVIYVQR-UHFFFAOYSA-N 2-(3-bromopropyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCCBr)C(=O)C2=C1 VKJCJJYNVIYVQR-UHFFFAOYSA-N 0.000 claims 2
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims 2
TXFPEBPIARQUIG-UHFFFAOYSA-N 4'-hydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1 TXFPEBPIARQUIG-UHFFFAOYSA-N 0.000 claims 2
NPFYZDNDJHZQKY-UHFFFAOYSA-N 4-Hydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 NPFYZDNDJHZQKY-UHFFFAOYSA-N 0.000 claims 2
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims 2
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims 2
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims 2
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims 2
SRUISGSHWFJION-UHFFFAOYSA-N E-4031 Chemical compound CC1=CC=CC(CCN2CCC(CC2)C(=O)C=2C=CC(NS(C)(=O)=O)=CC=2)=N1 SRUISGSHWFJION-UHFFFAOYSA-N 0.000 claims 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 2
TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims 2
241001465754 Metazoa Species 0.000 claims 2
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims 2
229910002651 NO3 Inorganic materials 0.000 claims 2
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims 2
229910019142 PO4 Inorganic materials 0.000 claims 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 2
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims 2
206010049418 Sudden Cardiac Death Diseases 0.000 claims 2
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 2
206010047281 Ventricular arrhythmia Diseases 0.000 claims 2
235000019270 ammonium chloride Nutrition 0.000 claims 2
239000008346 aqueous phase Substances 0.000 claims 2
206010003119 arrhythmia Diseases 0.000 claims 2
125000004429 atom Chemical group 0.000 claims 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 2
239000002775 capsule Substances 0.000 claims 2
230000000747 cardiac effect Effects 0.000 claims 2
239000003153 chemical reaction reagent Substances 0.000 claims 2
238000003776 cleavage reaction Methods 0.000 claims 2
239000012043 crude product Substances 0.000 claims 2
230000003111 delayed effect Effects 0.000 claims 2
230000037024 effective refractory period Effects 0.000 claims 2
DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical compound O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 claims 2
238000010438 heat treatment Methods 0.000 claims 2
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LRYIAUVHMBGMQE-UHFFFAOYSA-N 4-[4-[(4-methylphenyl)sulfonylamino]butoxy]benzenecarbothioamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NCCCCOC1=CC=C(C(N)=S)C=C1 LRYIAUVHMBGMQE-UHFFFAOYSA-N 0.000 claims 1
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ATDYDSYGGBABGY-UHFFFAOYSA-N 4-bromo-n-[4-[4-(tetrazol-1-yl)phenoxy]butyl]benzenesulfonamide Chemical group C1=CC(Br)=CC=C1S(=O)(=O)NCCCCOC1=CC=C(N2N=NN=C2)C=C1 ATDYDSYGGBABGY-UHFFFAOYSA-N 0.000 claims 1
ASMJPRUEKJPTHS-UHFFFAOYSA-N 4-bromo-n-[5-(4-imidazol-1-ylphenoxy)pentyl]benzenesulfonamide Chemical group C1=CC(Br)=CC=C1S(=O)(=O)NCCCCCOC1=CC=C(N2C=NC=C2)C=C1 ASMJPRUEKJPTHS-UHFFFAOYSA-N 0.000 claims 1
DRSPQRABKITGGB-UHFFFAOYSA-N 4-butoxy-n-[4-(4-imidazol-1-ylphenoxy)butyl]benzenesulfonamide Chemical group C1=CC(OCCCC)=CC=C1S(=O)(=O)NCCCCOC1=CC=C(N2C=NC=C2)C=C1 DRSPQRABKITGGB-UHFFFAOYSA-N 0.000 claims 1
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CZHOPESURGXOST-UHFFFAOYSA-N 4-chloro-2-[4-(4-imidazol-1-ylphenoxy)butyl]benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=C(Cl)C=C1CCCCOC1=CC=C(N2C=NC=C2)C=C1 CZHOPESURGXOST-UHFFFAOYSA-N 0.000 claims 1
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ORQQCFSNVXXGPI-UHFFFAOYSA-N 4-cyano-n-[4-(4-imidazol-1-ylphenoxy)butyl]benzenesulfonamide Chemical compound C=1C=C(C#N)C=CC=1S(=O)(=O)NCCCCOC(C=C1)=CC=C1N1C=CN=C1 ORQQCFSNVXXGPI-UHFFFAOYSA-N 0.000 claims 1
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CVNOWLNNPYYEOH-UHFFFAOYSA-N 4-cyanophenol Chemical compound OC1=CC=C(C#N)C=C1 CVNOWLNNPYYEOH-UHFFFAOYSA-N 0.000 claims 1
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CZKLEJHVLCMVQR-UHFFFAOYSA-N 4-fluorobenzoyl chloride Chemical compound FC1=CC=C(C(Cl)=O)C=C1 CZKLEJHVLCMVQR-UHFFFAOYSA-N 0.000 claims 1
POXFXTSTVWDWIR-UHFFFAOYSA-N 4-iodobenzenesulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=C(I)C=C1 POXFXTSTVWDWIR-UHFFFAOYSA-N 0.000 claims 1
NJAKCIUOTIPYED-UHFFFAOYSA-N 4-iodobenzoyl chloride Chemical compound ClC(=O)C1=CC=C(I)C=C1 NJAKCIUOTIPYED-UHFFFAOYSA-N 0.000 claims 1
DTJVECUKADWGMO-UHFFFAOYSA-N 4-methoxybenzenesulfonyl chloride Chemical compound COC1=CC=C(S(Cl)(=O)=O)C=C1 DTJVECUKADWGMO-UHFFFAOYSA-N 0.000 claims 1
LMVFMSMZCMRSEY-UHFFFAOYSA-N 4-methyl-n-[4-[4-(2h-tetrazol-5-yl)phenoxy]butyl]benzenesulfonamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NCCCCOC1=CC=C(C=2NN=NN=2)C=C1 LMVFMSMZCMRSEY-UHFFFAOYSA-N 0.000 claims 1
VEZCVJOXCLIKAZ-UHFFFAOYSA-N 4-methyl-n-[4-[4-(tetrazol-1-yl)phenoxy]butyl]benzenesulfonamide Chemical group C1=CC(C)=CC=C1S(=O)(=O)NCCCCOC1=CC=C(N2N=NN=C2)C=C1 VEZCVJOXCLIKAZ-UHFFFAOYSA-N 0.000 claims 1
NQUVCRCCRXRJCK-UHFFFAOYSA-N 4-methylbenzoyl chloride Chemical compound CC1=CC=C(C(Cl)=O)C=C1 NQUVCRCCRXRJCK-UHFFFAOYSA-N 0.000 claims 1
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FCQKPXLWWUGXCV-UHFFFAOYSA-N 4-tert-butyl-n-[4-(4-imidazol-1-ylphenoxy)butyl]benzenesulfonamide Chemical group C1=CC(C(C)(C)C)=CC=C1S(=O)(=O)NCCCCOC1=CC=C(N2C=NC=C2)C=C1 FCQKPXLWWUGXCV-UHFFFAOYSA-N 0.000 claims 1
YEZADZMMVHWFIY-UHFFFAOYSA-N 4-tert-butylbenzenesulfonyl chloride Chemical compound CC(C)(C)C1=CC=C(S(Cl)(=O)=O)C=C1 YEZADZMMVHWFIY-UHFFFAOYSA-N 0.000 claims 1
PMJXCXPDUMCWLB-UHFFFAOYSA-N 5-(aminomethyl)-n-[4-(4-imidazol-1-ylphenoxy)butyl]thiophene-2-sulfonamide Chemical compound S1C(CN)=CC=C1S(=O)(=O)NCCCCOC1=CC=C(N2C=NC=C2)C=C1 PMJXCXPDUMCWLB-UHFFFAOYSA-N 0.000 claims 1
VGSWVDWOXYTAPG-UHFFFAOYSA-N 5-(benzamidomethyl)thiophene-2-sulfonyl chloride Chemical compound S1C(S(=O)(=O)Cl)=CC=C1CNC(=O)C1=CC=CC=C1 VGSWVDWOXYTAPG-UHFFFAOYSA-N 0.000 claims 1
PCRODLZZZPRWHB-UHFFFAOYSA-N 5-phenoxy-1h-imidazole Chemical compound C=1C=CC=CC=1OC1=CNC=N1 PCRODLZZZPRWHB-UHFFFAOYSA-N 0.000 claims 1
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SYOCHRVVTJBVMF-UHFFFAOYSA-N n-[5-(4-imidazol-1-ylphenoxy)pentyl]hexane-1-sulfonamide Chemical compound C1=CC(OCCCCCNS(=O)(=O)CCCCCC)=CC=C1N1C=NC=C1 SYOCHRVVTJBVMF-UHFFFAOYSA-N 0.000 claims 1
LBTPIFQNEKOAIM-UHFFFAOYSA-N n-phenylmethanesulfonamide Chemical compound CS(=O)(=O)NC1=CC=CC=C1 LBTPIFQNEKOAIM-UHFFFAOYSA-N 0.000 claims 1
NSNPSJGHTQIXDO-UHFFFAOYSA-N naphthalene-1-carbonyl chloride Chemical compound C1=CC=C2C(C(=O)Cl)=CC=CC2=C1 NSNPSJGHTQIXDO-UHFFFAOYSA-N 0.000 claims 1
230000003957 neurotransmitter release Effects 0.000 claims 1
230000007935 neutral effect Effects 0.000 claims 1
239000002736 nonionic surfactant Substances 0.000 claims 1
WIVNTNLDTMNDNO-UHFFFAOYSA-N octane-1-sulfonyl chloride Chemical compound CCCCCCCCS(Cl)(=O)=O WIVNTNLDTMNDNO-UHFFFAOYSA-N 0.000 claims 1
150000007524 organic acids Chemical class 0.000 claims 1
230000003647 oxidation Effects 0.000 claims 1
238000007254 oxidation reaction Methods 0.000 claims 1
230000001590 oxidative effect Effects 0.000 claims 1
125000004430 oxygen atom Chemical group O* 0.000 claims 1
239000000312 peanut oil Substances 0.000 claims 1
229940043200 pentothal Drugs 0.000 claims 1
230000010412 perfusion Effects 0.000 claims 1
150000004965 peroxy acids Chemical class 0.000 claims 1
LIGACIXOYTUXAW-UHFFFAOYSA-N phenacyl bromide Chemical compound BrCC(=O)C1=CC=CC=C1 LIGACIXOYTUXAW-UHFFFAOYSA-N 0.000 claims 1
ULSIYEODSMZIPX-UHFFFAOYSA-N phenylethanolamine Chemical class NCC(O)C1=CC=CC=C1 ULSIYEODSMZIPX-UHFFFAOYSA-N 0.000 claims 1
ABOYDMHGKWRPFD-UHFFFAOYSA-N phenylmethanesulfonamide Chemical compound NS(=O)(=O)CC1=CC=CC=C1 ABOYDMHGKWRPFD-UHFFFAOYSA-N 0.000 claims 1
OAHKWDDSKCRNFE-UHFFFAOYSA-N phenylmethanesulfonyl chloride Chemical compound ClS(=O)(=O)CC1=CC=CC=C1 OAHKWDDSKCRNFE-UHFFFAOYSA-N 0.000 claims 1
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 1
PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical compound NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 claims 1
150000003109 potassium Chemical class 0.000 claims 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims 1
FYRHIOVKTDQVFC-UHFFFAOYSA-M potassium phthalimide Chemical compound [K+].C1=CC=C2C(=O)[N-]C(=O)C2=C1 FYRHIOVKTDQVFC-UHFFFAOYSA-M 0.000 claims 1
159000000001 potassium salts Chemical class 0.000 claims 1
230000001376 precipitating effect Effects 0.000 claims 1
230000002335 preservative effect Effects 0.000 claims 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims 1
210000003742 purkinje fiber Anatomy 0.000 claims 1
229960001404 quinidine Drugs 0.000 claims 1
JUYUYCIJACTHMK-UHFFFAOYSA-N quinoline-8-sulfonyl chloride Chemical compound C1=CN=C2C(S(=O)(=O)Cl)=CC=CC2=C1 JUYUYCIJACTHMK-UHFFFAOYSA-N 0.000 claims 1
230000009467 reduction Effects 0.000 claims 1
230000000717 retained effect Effects 0.000 claims 1
238000012552 review Methods 0.000 claims 1
230000033764 rhythmic process Effects 0.000 claims 1
210000005241 right ventricle Anatomy 0.000 claims 1
239000008159 sesame oil Substances 0.000 claims 1
235000011803 sesame oil Nutrition 0.000 claims 1
229910052708 sodium Inorganic materials 0.000 claims 1
239000003195 sodium channel blocking agent Substances 0.000 claims 1
239000011780 sodium chloride Substances 0.000 claims 1
159000000000 sodium salts Chemical class 0.000 claims 1
239000008247 solid mixture Substances 0.000 claims 1
239000008107 starch Substances 0.000 claims 1
235000019698 starch Nutrition 0.000 claims 1
239000008223 sterile water Substances 0.000 claims 1
230000004936 stimulating effect Effects 0.000 claims 1
239000000126 substance Substances 0.000 claims 1
239000005720 sucrose Substances 0.000 claims 1
125000000446 sulfanediyl group Chemical group *S* 0.000 claims 1
150000003457 sulfones Chemical class 0.000 claims 1
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
150000003462 sulfoxides Chemical class 0.000 claims 1
239000004094 surface-active agent Substances 0.000 claims 1
235000020357 syrup Nutrition 0.000 claims 1
239000006188 syrup Substances 0.000 claims 1
239000011975 tartaric acid Substances 0.000 claims 1
235000002906 tartaric acid Nutrition 0.000 claims 1
230000004797 therapeutic response Effects 0.000 claims 1
VNNLHYZDXIBHKZ-UHFFFAOYSA-N thiophene-2-sulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CS1 VNNLHYZDXIBHKZ-UHFFFAOYSA-N 0.000 claims 1
230000007306 turnover Effects 0.000 claims 1
235000015112 vegetable and seed oil Nutrition 0.000 claims 1
239000008158 vegetable oil Substances 0.000 claims 1
208000003663 ventricular fibrillation Diseases 0.000 claims 1
206010047302 ventricular tachycardia Diseases 0.000 claims 1
235000019165 vitamin E Nutrition 0.000 claims 1
229940046009 vitamin E Drugs 0.000 claims 1
239000011709 vitamin E Substances 0.000 claims 1
238000005303 weighing Methods 0.000 claims 1
229910052727 yttrium Inorganic materials 0.000 claims 1
238000009434 installation Methods 0.000 description 11
238000010276 construction Methods 0.000 description 5
238000011010 flushing procedure Methods 0.000 description 4
238000005253 cladding Methods 0.000 description 3
230000006978 adaptation Effects 0.000 description 2
238000005260 corrosion Methods 0.000 description 2
230000007797 corrosion Effects 0.000 description 2
238000003780 insertion Methods 0.000 description 2
230000037431 insertion Effects 0.000 description 2
239000000463 material Substances 0.000 description 2
239000011449 brick Substances 0.000 description 1
210000001520 comb Anatomy 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
238000010292 electrical insulation Methods 0.000 description 1
238000005304 joining Methods 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
238000005192 partition Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1

Classifications

- E—FIXED CONSTRUCTIONS
- E03—WATER SUPPLY; SEWERAGE
- E03D—WATER-CLOSETS OR URINALS WITH FLUSHING DEVICES; FLUSHING VALVES THEREFOR
- E03D11/00—Other component parts of water-closets, e.g. noise-reducing means in the flushing system, flushing pipes mounted in the bowl, seals for the bowl outlet, devices preventing overflow of the bowl contents; devices forming a water seal in the bowl after flushing, devices eliminating obstructions in the bowl outlet or preventing backflow of water and excrements from the waterpipe
- E03D11/13—Parts or details of bowls; Special adaptations of pipe joints or couplings for use with bowls, e.g. provisions in bowl construction preventing backflow of waste-water from the bowl in the flushing pipe or cistern, provisions for a secondary flushing, for noise-reducing
- E03D11/14—Means for connecting the bowl to the wall, e.g. to a wall outlet
- E03D11/143—Mounting frames for toilets and urinals
- E03D11/146—Mounting frames for toilets and urinals with incorporated cistern

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Hydrology & Water Resources (AREA)
Public Health (AREA)
Water Supply & Treatment (AREA)
Sanitary Device For Flush Toilet (AREA)
Adornments (AREA)
Orthopedics, Nursing, And Contraception (AREA)
Absorbent Articles And Supports Therefor (AREA)
Burglar Alarm Systems (AREA)
Bidet-Like Cleaning Device And Other Flush Toilet Accessories (AREA)

NO970685A 1996-02-16 1997-02-14 Festeanordning for et sanitærelement NO970685L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE29602714U DE29602714U1 (de)	1996-02-16	1996-02-16	Befestigungsvorrichtung für ein Sanitärelement

Publications (2)

Publication Number	Publication Date
NO970685D0 NO970685D0 (no)	1997-02-14
NO970685L true NO970685L (no)	1997-08-18

Family

ID=8019562

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO970685A NO970685L (no)	1996-02-16	1997-02-14	Festeanordning for et sanitærelement

Country Status (11)

Country	Link
EP (1)	EP0790359B1 (cs)
AT (1)	ATE224984T1 (cs)
AU (1)	AU727619B2 (cs)
CZ (1)	CZ35997A3 (cs)
DE (2)	DE29602714U1 (cs)
HR (1)	HRP970082A2 (cs)
IL (1)	IL120197A (cs)
MX (1)	MX9701101A (cs)
NO (1)	NO970685L (cs)
PL (1)	PL182550B1 (cs)
SK (1)	SK20497A3 (cs)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19736341C2 (de) *	1997-08-21	2002-09-19	Friatec Ag	Befestigungsvorrichtung
TW390925B (en) *	1998-02-18	2000-05-21	Inax Corp	Structure of arranging piping unit
DE19835789A1 (de) *	1998-08-07	2000-02-17	Friatec Ag	Vorrichtung zur Befestigung eines Bauelements
DE102007012251A1 (de) *	2007-03-14	2008-09-18	Trw Automotive Gmbh	Gassackmodul

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2249788A1 (de) *	1972-10-06	1974-04-11	Autokino Bau Gmbh	Sanitaerzelle
DE3309460A1 (de) *	1983-03-16	1984-09-27	Sanbloc GmbH Installations-Fertigbau, 8120 Weilheim	Geschaeumter installationsbaustein fuer sanitaerapparate
CH667121A5 (de) *	1985-03-08	1988-09-15	Geberit Ag	Haltevorrichtung fuer die vorwandmontage von sanitaerapparaten, armaturen, rohrteilen und leitungen.
GB2223042B (en) *	1988-09-26	1992-05-20	Frost F C Ltd	A mounting assembly
DE8902318U1 (de)	1989-02-27	1989-04-06	Wisan Technik AG, Zug	Sanitärelement zum Tragen eines Wand-WC
DE8914494U1 (de) *	1989-07-07	1990-01-25	Geberit Ag, Jona, St.Gallen	Montagerahmen für die Vorwandinstallation eines Sanitärapparates und insbesondere eines Urinals
DE9308693U1 (de) *	1992-07-20	1993-08-05	Geberit Ag, Jona, St.Gallen	Anschlußplatte zum Befestigen von beispielsweise sanitären Armaturen
DE9213588U1 (de) *	1992-10-08	1993-02-25	Kuhfuss Sanitär GmbH, 4901 Hiddenhausen	Installationsgestell für die Anbringung von Sanitärobjekten
DE4413776A1 (de) *	1994-02-08	1995-08-10	A & S Baeder Gmbh	System und Verfahren für die Sanitärinstallation
DE9412649U1 (de) *	1994-08-05	1994-11-10	Robert Plersch Edelstahl-Technik GmbH, 87749 Hawangen	Rahmen für die Vorwandmontage von sanitären Einrichtungen
DE9414960U1 (de) *	1994-09-15	1994-11-17	Zako Installationsfertigelemente Gmbh, 32758 Detmold	Installationsblock
DE29501299U1 (de) *	1995-01-27	1995-03-09	Ferroplast GmbH, 40789 Monheim	Montagerahmen für Sanitärkörper

1996
- 1996-02-16 DE DE29602714U patent/DE29602714U1/de not_active Expired - Lifetime
1997
- 1997-02-04 AT AT97101688T patent/ATE224984T1/de not_active IP Right Cessation
- 1997-02-04 EP EP97101688A patent/EP0790359B1/de not_active Expired - Lifetime
- 1997-02-04 DE DE59708293T patent/DE59708293D1/de not_active Expired - Fee Related
- 1997-02-06 CZ CZ97359A patent/CZ35997A3/cs unknown
- 1997-02-11 AU AU12626/97A patent/AU727619B2/en not_active Ceased
- 1997-02-11 IL IL12019797A patent/IL120197A/xx not_active IP Right Cessation
- 1997-02-12 SK SK204-97A patent/SK20497A3/sk unknown
- 1997-02-12 MX MX9701101A patent/MX9701101A/es unknown
- 1997-02-13 HR HR29602714.6A patent/HRP970082A2/hr not_active Application Discontinuation
- 1997-02-14 NO NO970685A patent/NO970685L/no not_active Application Discontinuation
- 1997-02-14 PL PL97318492A patent/PL182550B1/pl not_active IP Right Cessation

Also Published As

Publication number	Publication date
SK20497A3 (en)	1997-11-05
EP0790359A1 (de)	1997-08-20
AU727619B2 (en)	2000-12-14
DE29602714U1 (de)	1996-04-18
EP0790359B1 (de)	2002-09-25
NO970685D0 (no)	1997-02-14
PL182550B1 (pl)	2002-01-31
IL120197A0 (en)	1997-06-10
ATE224984T1 (de)	2002-10-15
AU1262697A (en)	1997-08-21
PL318492A1 (en)	1997-08-18
DE59708293D1 (de)	2002-10-31
MX9701101A (es)	1997-08-30
IL120197A (en)	1999-12-31
CZ35997A3 (en)	1997-11-12
HRP970082A2 (en)	1998-02-28

Legal Events

Date	Code	Title	Description
2003-10-27	FC2A	Withdrawal, rejection or dismissal of laid open patent application

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