NL7902829A - Di- en tri-isotazuurderivaten, hun bereiding en toepassing. - Google Patents

Di- en tri-isotazuurderivaten, hun bereiding en toepassing. Download PDF

Info

Publication number: NL7902829A
Authority: NL; Netherlands
Prior art keywords: formula; group; compound; compounds; carbon atoms
Prior art date: 1979-04-10

Application number

NL7902829A

Other languages

English (en)

Dutch (nl)

Original Assignee

Lim Holding Sa

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.)

1979-04-10

Filing date

1979-04-10

Publication date

1980-10-14

1979-04-10 Application filed by Lim Holding Sa filed Critical Lim Holding Sa

1979-04-10 Priority to ZA791723A priority Critical patent/ZA791723B/xx

1979-04-10 Priority to BE0/194501A priority patent/BE875452A/fr

1979-04-10 Priority to AU45999/79A priority patent/AU4599979A/en

1979-04-10 Priority to SE7903189A priority patent/SE7903189L/xx

1979-04-10 Priority to FR7909078A priority patent/FR2453856A1/fr

1979-04-10 Priority to IT21741/79A priority patent/IT1111921B/it

1979-04-10 Priority to JP4356679A priority patent/JPS55139345A/ja

1979-04-10 Priority to GB7912634A priority patent/GB2046244A/en

1979-04-10 Priority to DD79212125A priority patent/DD143609A5/de

1979-04-10 Priority to BR7902207A priority patent/BR7902207A/pt

1979-04-10 Priority to NL7902829A priority patent/NL7902829A/nl

1979-04-10 Priority to US06/028,754 priority patent/US4283548A/en

1979-04-10 Priority to DE19792914545 priority patent/DE2914545A1/de

1980-10-14 Publication of NL7902829A publication Critical patent/NL7902829A/nl

Links

238000002360 preparation method Methods 0.000 title claims description 26
239000002253 acid Substances 0.000 title description 6
150000001875 compounds Chemical class 0.000 claims description 61
229920001228 polyisocyanate Polymers 0.000 claims description 46
239000005056 polyisocyanate Substances 0.000 claims description 46
VYFOAVADNIHPTR-UHFFFAOYSA-N isatoic anhydride Chemical compound NC1=CC=CC=C1CO VYFOAVADNIHPTR-UHFFFAOYSA-N 0.000 claims description 19
125000004432 carbon atom Chemical group C* 0.000 claims description 17
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 14
239000012948 isocyanate Substances 0.000 claims description 14
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 14
229920003023 plastic Polymers 0.000 claims description 14
239000004033 plastic Substances 0.000 claims description 14
150000002513 isocyanates Chemical class 0.000 claims description 13
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 12
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 12
239000001301 oxygen Substances 0.000 claims description 12
229910052760 oxygen Inorganic materials 0.000 claims description 12
229910052717 sulfur Inorganic materials 0.000 claims description 12
239000011593 sulfur Substances 0.000 claims description 12
238000006243 chemical reaction Methods 0.000 claims description 11
238000000034 method Methods 0.000 claims description 11
-1 phenylenedioxy group Chemical group 0.000 claims description 11
239000004814 polyurethane Substances 0.000 claims description 11
229920002635 polyurethane Polymers 0.000 claims description 11
125000001424 substituent group Chemical group 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 10
125000002947 alkylene group Chemical group 0.000 claims description 10
239000001257 hydrogen Substances 0.000 claims description 8
229910052739 hydrogen Inorganic materials 0.000 claims description 8
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 7
239000005977 Ethylene Substances 0.000 claims description 7
239000000203 mixture Substances 0.000 claims description 7
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
125000001118 alkylidene group Chemical group 0.000 claims description 4
239000003054 catalyst Substances 0.000 claims description 4
150000002009 diols Chemical class 0.000 claims description 4
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 4
125000000623 heterocyclic group Chemical group 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 4
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 4
229920002396 Polyurea Polymers 0.000 claims description 3
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 claims description 3
239000000654 additive Substances 0.000 claims description 3
239000003063 flame retardant Substances 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims description 2
239000003960 organic solvent Substances 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
229920000162 poly(ureaurethane) Polymers 0.000 claims description 2
125000005842 heteroatom Chemical group 0.000 claims 2
IFVTZJHWGZSXFD-UHFFFAOYSA-N biphenylene Chemical compound C1=CC=C2C3=CC=CC=C3C2=C1 IFVTZJHWGZSXFD-UHFFFAOYSA-N 0.000 claims 1
229940125904 compound 1 Drugs 0.000 claims 1
239000000945 filler Substances 0.000 claims 1
125000004430 oxygen atom Chemical group O* 0.000 claims 1
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 18
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical group NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 11
239000013078 crystal Substances 0.000 description 10
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 8
239000000741 silica gel Substances 0.000 description 8
229910002027 silica gel Inorganic materials 0.000 description 8
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical group CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
239000000706 filtrate Substances 0.000 description 6
235000011118 potassium hydroxide Nutrition 0.000 description 6
XYKIUTSFQGXHOW-UHFFFAOYSA-N propan-2-one;toluene Chemical compound CC(C)=O.CC1=CC=CC=C1 XYKIUTSFQGXHOW-UHFFFAOYSA-N 0.000 description 6
150000002148 esters Chemical class 0.000 description 5
239000011541 reaction mixture Substances 0.000 description 5
238000003756 stirring Methods 0.000 description 5
238000004809 thin layer chromatography Methods 0.000 description 5
239000004970 Chain extender Substances 0.000 description 4
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
238000004458 analytical method Methods 0.000 description 4
230000002349 favourable effect Effects 0.000 description 4
239000002244 precipitate Substances 0.000 description 4
229910052938 sodium sulfate Inorganic materials 0.000 description 4
235000011152 sodium sulphate Nutrition 0.000 description 4
239000007858 starting material Substances 0.000 description 4
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
238000002425 crystallisation Methods 0.000 description 3
230000008025 crystallization Effects 0.000 description 3
150000004985 diamines Chemical class 0.000 description 3
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
235000011121 sodium hydroxide Nutrition 0.000 description 3
238000010626 work up procedure Methods 0.000 description 3
ATIAIEWDRRJGSL-UHFFFAOYSA-N 1,3-bis(2-hydroxyethyl)-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(CCO)C(=O)N(CCO)C1=O ATIAIEWDRRJGSL-UHFFFAOYSA-N 0.000 description 2
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 2
239000002198 insoluble material Substances 0.000 description 2
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
229960005323 phenoxyethanol Drugs 0.000 description 2
239000011591 potassium Substances 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
239000000047 product Substances 0.000 description 2
238000010992 reflux Methods 0.000 description 2
AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 2
125000003837 (C1-C20) alkyl group Chemical group 0.000 description 1
FOEPCDLNKFULCQ-UHFFFAOYSA-N 1,3-bis(2-chloroethyl)-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(CCCl)C(=O)N(CCCl)C1=O FOEPCDLNKFULCQ-UHFFFAOYSA-N 0.000 description 1
OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 description 1
SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
RFQGAFQKNITSIA-UHFFFAOYSA-N 2-(carboxyamino)benzoic acid Chemical class OC(=O)NC1=CC=CC=C1C(O)=O RFQGAFQKNITSIA-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
YIROYDNZEPTFOL-UHFFFAOYSA-N 5,5-Dimethylhydantoin Chemical compound CC1(C)NC(=O)NC1=O YIROYDNZEPTFOL-UHFFFAOYSA-N 0.000 description 1
241000234282 Allium Species 0.000 description 1
235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
FVIGODVHAVLZOO-UHFFFAOYSA-N Dixanthogen Chemical compound CCOC(=S)SSC(=S)OCC FVIGODVHAVLZOO-UHFFFAOYSA-N 0.000 description 1
238000005684 Liebig rearrangement reaction Methods 0.000 description 1
UNNGDHMFFIUHLS-UHFFFAOYSA-N SCCOC1(CC=CC=C1)OCCS Chemical compound SCCOC1(CC=CC=C1)OCCS UNNGDHMFFIUHLS-UHFFFAOYSA-N 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
238000010306 acid treatment Methods 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000003368 amide group Chemical group 0.000 description 1
125000003277 amino group Chemical class 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
150000001448 anilines Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
230000000711 cancerogenic effect Effects 0.000 description 1
238000005266 casting Methods 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
229940126214 compound 3 Drugs 0.000 description 1
238000010276 construction Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
238000010586 diagram Methods 0.000 description 1
JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 description 1
125000004185 ester group Chemical group 0.000 description 1
NDUXAYZFYGZISK-UHFFFAOYSA-N ethanol;propan-2-one;hydrate Chemical compound O.CCO.CC(C)=O NDUXAYZFYGZISK-UHFFFAOYSA-N 0.000 description 1
OAMZXMDZZWGPMH-UHFFFAOYSA-N ethyl acetate;toluene Chemical compound CCOC(C)=O.CC1=CC=CC=C1 OAMZXMDZZWGPMH-UHFFFAOYSA-N 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000012467 final product Substances 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
229940091173 hydantoin Drugs 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
XONPDZSGENTBNJ-UHFFFAOYSA-N molecular hydrogen;sodium Chemical compound [Na].[H][H] XONPDZSGENTBNJ-UHFFFAOYSA-N 0.000 description 1
NTTOTNSKUYCDAV-UHFFFAOYSA-N potassium hydride Chemical compound [KH] NTTOTNSKUYCDAV-UHFFFAOYSA-N 0.000 description 1
229910000105 potassium hydride Inorganic materials 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
HYHCSLBZRBJJCH-UHFFFAOYSA-M sodium hydrosulfide Chemical compound [Na+].[SH-] HYHCSLBZRBJJCH-UHFFFAOYSA-M 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3819—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C327/00—Thiocarboxylic acids
- C07C327/20—Esters of monothiocarboxylic acids
- C07C327/28—Esters of monothiocarboxylic acids having sulfur atoms of esterified thiocarboxyl groups bound to carbon atoms of hydrocarbon radicals substituted by singly-bound oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/225—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/23—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/72—Two oxygen atoms, e.g. hydantoin
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/72—Two oxygen atoms, e.g. hydantoin
- C07D233/74—Two oxygen atoms, e.g. hydantoin with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to other ring members
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/72—Two oxygen atoms, e.g. hydantoin
- C07D233/76—Two oxygen atoms, e.g. hydantoin with substituted hydrocarbon radicals attached to the third ring carbon atom
- C07D233/78—Radicals substituted by oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/26—Oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D277/70—Sulfur atoms
- C07D277/76—Sulfur atoms attached to a second hetero atom
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3225—Polyamines
- C08G18/3237—Polyamines aromatic
- C08G18/3243—Polyamines aromatic containing two or more aromatic rings
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen

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Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Indole Compounds (AREA)
Polyurethanes Or Polyureas (AREA)

NL7902829A 1979-04-10 1979-04-10 Di- en tri-isotazuurderivaten, hun bereiding en toepassing. NL7902829A (nl)

Priority Applications (13)

Application Number	Priority Date	Filing Date	Title
ZA791723A ZA791723B (en)	1979-04-10	1979-04-10	Disatoic acid or triisatoic acid derivatives processes for their production and their use
BE0/194501A BE875452A (fr)	1979-04-10	1979-04-10	Nouveaux derives d'acides di- ou tri-isatiniques, procedes de realisation et modes d'application
AU45999/79A AU4599979A (en)	1979-04-10	1979-04-10	Diisatoic acid or triisatoic acid derivatives
SE7903189A SE7903189L (sv)	1979-04-10	1979-04-10	Di- eller triisatosyraderivat, forfarande for dess framstellning samt anvendning derav
FR7909078A FR2453856A1 (fr)	1979-04-10	1979-04-10	Nouveaux derives d'acides di- ou triisatiniques, procedes de realisation, et modes d'application
IT21741/79A IT1111921B (it)	1979-04-10	1979-04-10	Di-e/o tri-derivati dell'acido o-carbossifenilcarbammico,procedimento per la loro produzione e loro impiego
JP4356679A JPS55139345A (en)	1979-04-10	1979-04-10	Derivative of diisatoic acid or triisatoic acid and its manufacture and use
GB7912634A GB2046244A (en)	1979-04-10	1979-04-10	Novel diisatoic and triisatoic acid derivatives
DD79212125A DD143609A5 (de)	1979-04-10	1979-04-10	Verfahren zur herstellung von di-bzw.tri-isatosaeure-derivaten
BR7902207A BR7902207A (pt)	1979-04-10	1979-04-10	Compostos organicos,processo para sua preparacao e seu emprego
NL7902829A NL7902829A (nl)	1979-04-10	1979-04-10	Di- en tri-isotazuurderivaten, hun bereiding en toepassing.
US06/028,754 US4283548A (en)	1979-04-10	1979-04-10	Diisatoic acid or triisatoic acid derivatives
DE19792914545 DE2914545A1 (de)	1979-04-10	1979-04-10	Di- bzw. tri-isatosaeure-derivate, verfahren zu deren herstellung und deren verwendung

Applications Claiming Priority (26)

Application Number	Priority Date	Filing Date	Title
BR7902207		1979-04-10
ZA791723A ZA791723B (en)	1979-04-10	1979-04-10	Disatoic acid or triisatoic acid derivatives processes for their production and their use
BE0/194501A BE875452A (fr)	1979-04-10	1979-04-10	Nouveaux derives d'acides di- ou tri-isatiniques, procedes de realisation et modes d'application
AU45999/79A AU4599979A (en)	1979-04-10	1979-04-10	Diisatoic acid or triisatoic acid derivatives
US2875479		1979-04-10
SE7903189A SE7903189L (sv)	1979-04-10	1979-04-10	Di- eller triisatosyraderivat, forfarande for dess framstellning samt anvendning derav
FR7909078A FR2453856A1 (fr)	1979-04-10	1979-04-10	Nouveaux derives d'acides di- ou triisatiniques, procedes de realisation, et modes d'application
IT21741/79A IT1111921B (it)	1979-04-10	1979-04-10	Di-e/o tri-derivati dell'acido o-carbossifenilcarbammico,procedimento per la loro produzione e loro impiego
JP4356679A JPS55139345A (en)	1979-04-10	1979-04-10	Derivative of diisatoic acid or triisatoic acid and its manufacture and use
JP4356679		1979-04-10
DE2914545		1979-04-10
DD21212579		1979-04-10
GB7912634A GB2046244A (en)	1979-04-10	1979-04-10	Novel diisatoic and triisatoic acid derivatives
DD79212125A DD143609A5 (de)	1979-04-10	1979-04-10	Verfahren zur herstellung von di-bzw.tri-isatosaeure-derivaten
GB7912634		1979-04-10
IT2174179		1979-04-10
BR7902207A BR7902207A (pt)	1979-04-10	1979-04-10	Compostos organicos,processo para sua preparacao e seu emprego
AU4599979		1979-04-10
FR7909078		1979-04-10
NL7902829A NL7902829A (nl)	1979-04-10	1979-04-10	Di- en tri-isotazuurderivaten, hun bereiding en toepassing.
US06/028,754 US4283548A (en)	1979-04-10	1979-04-10	Diisatoic acid or triisatoic acid derivatives
NL7902829		1979-04-10
SE7903189		1979-04-10
DE19792914545 DE2914545A1 (de)	1979-04-10	1979-04-10	Di- bzw. tri-isatosaeure-derivate, verfahren zu deren herstellung und deren verwendung
BE194501		1979-04-10
ZA7901723		1979-04-10

Publications (1)

Publication Number	Publication Date
NL7902829A true NL7902829A (nl)	1980-10-14

Family

ID=27583886

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL7902829A NL7902829A (nl)	1979-04-10	1979-04-10	Di- en tri-isotazuurderivaten, hun bereiding en toepassing.

Country Status (13)

Country	Link
US (1)	US4283548A (fr)
JP (1)	JPS55139345A (fr)
AU (1)	AU4599979A (fr)
BE (1)	BE875452A (fr)
BR (1)	BR7902207A (fr)
DD (1)	DD143609A5 (fr)
DE (1)	DE2914545A1 (fr)
FR (1)	FR2453856A1 (fr)
GB (1)	GB2046244A (fr)
IT (1)	IT1111921B (fr)
NL (1)	NL7902829A (fr)
SE (1)	SE7903189L (fr)
ZA (1)	ZA791723B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
KR102505374B1 (ko) *	2016-10-06	2023-03-02	닛산 가가쿠 가부시키가이샤	디아민, 중합체, 액정 배향제, 액정 배향막 및 액정 표시 소자
KR102980361B1 (ko)	2019-01-28	2026-06-23	닛산 가가쿠 가부시키가이샤	슬릿 다이 코트용 박리층 형성용 조성물 및 박리층
CN115537171A (zh) *	2022-09-27	2022-12-30	江苏华大新材料有限公司	一种耐低温聚氨酯复合胶及其制备方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4161594A (en) *	1968-11-11	1979-07-17	Ciba-Geigy Ag	Dialcohols
CH523279A (de) *	1968-11-11	1972-05-31	Ciba Geigy Ag	Verfahren zur Herstellung von neuen Diglycidylverbindungen von N-heterocyclischen Verbindungen und deren Verwendung
FR2148868A6 (fr) *	1970-10-06	1973-03-23	Rhone Poulenc Sa
CH546798A (de) *	1971-08-17	1974-03-15	Ciba Geigy Ag	Verfahren zum haerten von acrylsaeureesterderivaten mit ionisierenden strahlen.
CH570379A5 (fr) *	1972-07-12	1975-12-15	Ciba Geigy Ag
DD127235A5 (fr) *	1975-10-27	1977-09-14
US4129741A (en) *	1975-10-27	1978-12-12	Lim-Holding, S.A.	Novel polyethers having terminal amino groups, a process for their production and their application
US4122276A (en) *	1976-05-12	1978-10-24	Ciba-Geigy Corporation	Dicarboxylic acids and dicarboxylic acid esters containing a heterocyclic radical

1979
- 1979-04-10 ZA ZA791723A patent/ZA791723B/xx unknown
- 1979-04-10 US US06/028,754 patent/US4283548A/en not_active Expired - Lifetime
- 1979-04-10 AU AU45999/79A patent/AU4599979A/en not_active Abandoned
- 1979-04-10 SE SE7903189A patent/SE7903189L/xx not_active Application Discontinuation
- 1979-04-10 FR FR7909078A patent/FR2453856A1/fr not_active Withdrawn
- 1979-04-10 GB GB7912634A patent/GB2046244A/en not_active Withdrawn
- 1979-04-10 DE DE19792914545 patent/DE2914545A1/de not_active Ceased
- 1979-04-10 BR BR7902207A patent/BR7902207A/pt unknown
- 1979-04-10 DD DD79212125A patent/DD143609A5/de unknown
- 1979-04-10 JP JP4356679A patent/JPS55139345A/ja active Pending
- 1979-04-10 BE BE0/194501A patent/BE875452A/fr unknown
- 1979-04-10 IT IT21741/79A patent/IT1111921B/it active
- 1979-04-10 NL NL7902829A patent/NL7902829A/nl not_active Application Discontinuation

Also Published As

Publication number	Publication date
FR2453856A1 (fr)	1980-11-07
GB2046244A (en)	1980-11-12
DE2914545A1 (de)	1980-10-16
DD143609A5 (de)	1980-09-03
ZA791723B (en)	1980-04-30
JPS55139345A (en)	1980-10-31
IT7921741A0 (it)	1979-04-10
BR7902207A (pt)	1980-10-21
BE875452A (fr)	1979-10-10
US4283548A (en)	1981-08-11
AU4599979A (en)	1980-10-16
IT1111921B (it)	1986-01-13
SE7903189L (sv)	1980-10-11

Legal Events

Date	Code	Title	Description
1983-12-01	BV	The patent application has lapsed

Publication	Publication Date	Title
US3567763A (en)	1971-03-02	Ester polyisocyanates
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US4174455A (en)	1979-11-13	Anthranilates of oxyalkylated carboxamides
US4007239A (en)	1977-02-08	Aromatic diamines
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US4100348A (en)	1978-07-11	Triols containing hydantoin rings
US4124545A (en)	1978-11-07	Carbamic acid esters as catalysts for trimerization of isocyanates
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US4243756A (en)	1981-01-06	Stable-liquid isocyanurate-modified polyisocyanate compositions
US4259255A (en)	1981-03-31	Process for the production of isocyanates
US4576747A (en)	1986-03-18	Isocyanato-azetidinediones
US4229576A (en)	1980-10-21	Anthranilates of oxyalkylated cyanuric acid
US4342859A (en)	1982-08-03	Bis(aminophenylthioalkyl)terephthalate and hardener for polyurethane elastomer thereof
US4246425A (en)	1981-01-20	4-Chloro-3,5-diaminophenyl acetates and curing agent
US4139706A (en)	1979-02-13	Novel poly(thio)ethers having terminal amino groups, a process for their production and their application
US4339381A (en)	1982-07-13	1,3-Alkylene-diazetidine-2,4-diones
US4111918A (en)	1978-09-05	Polyparabanic acid derivatives
US4325887A (en)	1982-04-20	Isocyanatoaryl sulfonic acid esters
US4581435A (en)	1986-04-08	Alkyl-substituted thiapolycyclic polyahl and polyurethanes, polyamides and polyureas based thereon
US4170701A (en)	1979-10-09	Process for the preparation of (thio)hydantoins modified with amide groups
US5151524A (en)	1992-09-29	Process for preparing imidazolidine-2,5-dione derivative
US3985789A (en)	1976-10-12	Carbamic acid esters