IL33221A - Benzothiazole derivatives,preparation thereof and microbiocidal preparations containing them - Google Patents

Benzothiazole derivatives,preparation thereof and microbiocidal preparations containing them

Info

Publication number: IL33221A
Authority: IL; Israel
Prior art keywords: compound; formula; compounds; preparation; hydrogen
Prior art date: 1968-11-01

Application number

IL33221A

Other languages

English (en)

Other versions

IL33221A0 (en

Original Assignee

Cibageigy Ag

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.)

1968-11-01

Filing date

1969-10-20

Publication date

1973-06-29

1969-10-20 Application filed by Cibageigy Ag filed Critical Cibageigy Ag

1969-12-31 Publication of IL33221A0 publication Critical patent/IL33221A0/xx

1973-06-29 Publication of IL33221A publication Critical patent/IL33221A/en

Links

238000002360 preparation method Methods 0.000 title claims description 10
230000003641 microbiacidal effect Effects 0.000 title claims description 5
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 title description 3
150000001875 compounds Chemical class 0.000 claims description 23
239000004480 active ingredient Substances 0.000 claims description 10
238000004519 manufacturing process Methods 0.000 claims description 9
238000000034 method Methods 0.000 claims description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
241000233866 Fungi Species 0.000 claims description 5
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
241000894006 Bacteria Species 0.000 claims description 3
150000001412 amines Chemical class 0.000 claims description 3
230000003115 biocidal effect Effects 0.000 claims description 3
239000007787 solid Substances 0.000 claims description 3
125000001424 substituent group Chemical group 0.000 claims description 3
241000221576 Uromyces Species 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
239000007788 liquid Substances 0.000 claims description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
241000223600 Alternaria Species 0.000 claims 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
150000001722 carbon compounds Chemical class 0.000 claims 1
239000000460 chlorine Substances 0.000 claims 1
230000001717 pathogenic effect Effects 0.000 claims 1
239000013543 active substance Substances 0.000 description 13
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
241000196324 Embryophyta Species 0.000 description 6
230000002538 fungal effect Effects 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 5
239000008187 granular material Substances 0.000 description 5
238000005507 spraying Methods 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
239000000203 mixture Substances 0.000 description 4
239000000843 powder Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
239000005995 Aluminium silicate Substances 0.000 description 3
241000123650 Botrytis cinerea Species 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
241000221577 Uromyces appendiculatus Species 0.000 description 3
239000002253 acid Substances 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
235000010633 broth Nutrition 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
238000010410 dusting Methods 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
-1 for example Substances 0.000 description 3
150000002430 hydrocarbons Chemical class 0.000 description 3
159000000000 sodium salts Chemical class 0.000 description 3
239000000243 solution Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
229940126062 Compound A Drugs 0.000 description 2
240000008067 Cucumis sativus Species 0.000 description 2
241000896246 Golovinomyces cichoracearum Species 0.000 description 2
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
229960000892 attapulgite Drugs 0.000 description 2
238000009835 boiling Methods 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
238000011534 incubation Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000003921 oil Substances 0.000 description 2
229910052625 palygorskite Inorganic materials 0.000 description 2
239000000047 product Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
235000012222 talc Nutrition 0.000 description 2
235000013311 vegetables Nutrition 0.000 description 2
239000008096 xylene Chemical class 0.000 description 2
QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 1
ICLYJLBTOGPLMC-KVVVOXFISA-N (z)-octadec-9-enoate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCC\C=C/CCCCCCCC(O)=O ICLYJLBTOGPLMC-KVVVOXFISA-N 0.000 description 1
QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 1
GBDZXPJXOMHESU-UHFFFAOYSA-N 1,2,3,4-tetrachlorobenzene Chemical class ClC1=CC=C(Cl)C(Cl)=C1Cl GBDZXPJXOMHESU-UHFFFAOYSA-N 0.000 description 1
RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical class ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 1
QAQSNXHKHKONNS-UHFFFAOYSA-N 1-ethyl-2-hydroxy-4-methyl-6-oxopyridine-3-carboxamide Chemical compound CCN1C(O)=C(C(N)=O)C(C)=CC1=O QAQSNXHKHKONNS-UHFFFAOYSA-N 0.000 description 1
MKOHEKNXWUQXNQ-UHFFFAOYSA-N 2,2-dihydroxyethyl(13-phenyltridecyl)azanium;chloride Chemical compound [Cl-].OC(O)C[NH2+]CCCCCCCCCCCCCC1=CC=CC=C1 MKOHEKNXWUQXNQ-UHFFFAOYSA-N 0.000 description 1
UHGULLIUJBCTEF-UHFFFAOYSA-N 2-aminobenzothiazole Chemical class C1=CC=C2SC(N)=NC2=C1 UHGULLIUJBCTEF-UHFFFAOYSA-N 0.000 description 1
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
ISAVYTVYFVQUDY-UHFFFAOYSA-N 4-tert-Octylphenol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(O)C=C1 ISAVYTVYFVQUDY-UHFFFAOYSA-N 0.000 description 1
KOYJWFGMEBETBU-UHFFFAOYSA-N 6-ethoxy-1,3-benzothiazol-2-amine Chemical compound CCOC1=CC=C2N=C(N)SC2=C1 KOYJWFGMEBETBU-UHFFFAOYSA-N 0.000 description 1
BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
241000223602 Alternaria alternata Species 0.000 description 1
241000213004 Alternaria solani Species 0.000 description 1
DJHGAFSJWGLOIV-UHFFFAOYSA-K Arsenate3- Chemical class [O-][As]([O-])([O-])=O DJHGAFSJWGLOIV-UHFFFAOYSA-K 0.000 description 1
XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 1
235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
YIIMEMSDCNDGTB-UHFFFAOYSA-N Dimethylcarbamoyl chloride Chemical compound CN(C)C(Cl)=O YIIMEMSDCNDGTB-UHFFFAOYSA-N 0.000 description 1
241000221787 Erysiphe Species 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241001387976 Pera Species 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
238000007792 addition Methods 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000003463 adsorbent Substances 0.000 description 1
229920000615 alginic acid Polymers 0.000 description 1
235000010443 alginic acid Nutrition 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 1
GCPXMJHSNVMWNM-UHFFFAOYSA-N arsenous acid Chemical class O[As](O)O GCPXMJHSNVMWNM-UHFFFAOYSA-N 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
235000012216 bentonite Nutrition 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
150000001642 boronic acid derivatives Chemical class 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
235000010216 calcium carbonate Nutrition 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
229910000389 calcium phosphate Inorganic materials 0.000 description 1
235000011010 calcium phosphates Nutrition 0.000 description 1
HCWYXKWQOMTBKY-UHFFFAOYSA-N calcium;dodecyl benzenesulfonate Chemical compound [Ca].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 HCWYXKWQOMTBKY-UHFFFAOYSA-N 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
235000013877 carbamide Nutrition 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000005018 casein Substances 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
235000021240 caseins Nutrition 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000003610 charcoal Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
239000011280 coal tar Substances 0.000 description 1
239000007799 cork Substances 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical class OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
239000002283 diesel fuel Substances 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000009826 distribution Methods 0.000 description 1
WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
LQZZUXJYWNFBMV-UHFFFAOYSA-N ethyl butylhexanol Natural products CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
244000000004 fungal plant pathogen Species 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
239000003292 glue Substances 0.000 description 1
238000005469 granulation Methods 0.000 description 1
230000003179 granulation Effects 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002391 heterocyclic compounds Chemical class 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000002855 microbicide agent Substances 0.000 description 1
239000011707 mineral Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
150000003016 phosphoric acids Chemical class 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
239000001117 sulphuric acid Substances 0.000 description 1
235000011149 sulphuric acid Nutrition 0.000 description 1
239000000725 suspension Substances 0.000 description 1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical class C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

Classifications

- 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
- C07D277/82—Nitrogen atoms
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms

Landscapes

Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

IL33221A 1968-11-01 1969-10-20 Benzothiazole derivatives,preparation thereof and microbiocidal preparations containing them IL33221A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH1633368A CH505543A (de)	1968-11-01	1968-11-01	Schädlingsbekämpfungsmittel

Publications (2)

Publication Number	Publication Date
IL33221A0 IL33221A0 (en)	1969-12-31
IL33221A true IL33221A (en)	1973-06-29

Family

ID=4416400

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL33221A IL33221A (en)	1968-11-01	1969-10-20	Benzothiazole derivatives,preparation thereof and microbiocidal preparations containing them

Country Status (13)

Country	Link
US (1)	US3725428A (ro)
AT (1)	AT295922B (ro)
BE (1)	BE741093A (ro)
BG (1)	BG17439A3 (ro)
CH (1)	CH505543A (ro)
CS (1)	CS164834B2 (ro)
DE (1)	DE1953149A1 (ro)
DK (1)	DK128742B (ro)
FR (1)	FR2022369A1 (ro)
GB (1)	GB1290388A (ro)
IL (1)	IL33221A (ro)
NL (1)	NL6916457A (ro)
RO (1)	RO61385A (ro)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE787660A (fr) *	1971-08-19	1973-02-19	Bayer Ag	Nouvelles 1-(2-benzothiazolyl)1,3-dialkylurees, leur preparation et leur application comme herbicides
JPS5637205B2 (ro) *	1973-02-05	1981-08-29
AR204835A1 (es) *	1973-07-18	1976-03-05	Scherico Ltd	Procedimiento para preparar benzotiazol-2-carbamatos de etilo
US4006242A (en) *	1973-07-18	1977-02-01	Schering Corporation	Certain benzothiazoles used in the treatment of helminthiasis
DK148476C (da) *	1975-04-25	1985-12-16	Scherico Ltd	Analogifremgangsmaade til fremstilling af methyl-6-n-propoxybenzothiazol-2-carbamat
US4057638A (en) *	1975-07-03	1977-11-08	E. I. Du Pont De Nemours And Company	Benzothiazole allophanate fungicides
US4093731A (en) *	1976-03-30	1978-06-06	Schering Corporation	Methyl-6-n-propoxybenzothiazole-2-carbamate and anthelmintic pharmaceutical compositions thereof
US4380640A (en) *	1980-01-21	1983-04-19	Ciba-Geigy Corporation	Novel benzthiazolylurea derivatives, compositions containing them and their use as herbicides
DE59005183D1 (de) *	1989-11-10	1994-05-05	Agrolinz Agrarchemikalien	Verfahren zur Herstellung reiner, unsymmetrisch disubstituierter Harnstoffe.
DE3940261A1 (de) *	1989-12-06	1991-06-13	Agrolinz Agrarchemikalien Muen	Verfahren zur herstellung reiner, unsymmetrisch disubstituierter harnstoffe
WO2001057008A1 (en) *	2000-02-07	2001-08-09	Abbott Gesellschaft Mit Beschrankter Haftung & Company Kommanditgesellschaft	2-benzothiazolyl urea derivatives and their use as protein kinase inhibitors
NZ522928A (en)	2000-06-21	2005-05-27	F	Benzothiazole derivatives
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1968
- 1968-11-01 CH CH1633368A patent/CH505543A/de not_active IP Right Cessation
1969
- 1969-10-13 BG BG013177A patent/BG17439A3/xx unknown
- 1969-10-20 IL IL33221A patent/IL33221A/en unknown
- 1969-10-22 DE DE19691953149 patent/DE1953149A1/de active Pending
- 1969-10-22 US US00868589A patent/US3725428A/en not_active Expired - Lifetime
- 1969-10-27 GB GB1290388D patent/GB1290388A/en not_active Expired
- 1969-10-30 FR FR6937369A patent/FR2022369A1/fr not_active Withdrawn
- 1969-10-31 AT AT1027069A patent/AT295922B/de not_active IP Right Cessation
- 1969-10-31 NL NL6916457A patent/NL6916457A/xx unknown
- 1969-10-31 RO RO61433A patent/RO61385A/ro unknown
- 1969-10-31 CS CS7208A patent/CS164834B2/cs unknown
- 1969-10-31 BE BE741093D patent/BE741093A/xx unknown
- 1969-10-31 DK DK575369AA patent/DK128742B/da unknown

Also Published As

Publication number	Publication date
GB1290388A (ro)	1972-09-27
CH505543A (de)	1971-04-15
CS164834B2 (ro)	1975-11-28
RO61385A (ro)	1976-12-15
FR2022369A1 (ro)	1970-07-31
BE741093A (ro)	1970-04-30
US3725428A (en)	1973-04-03
BG17439A3 (bg)	1973-11-10
NL6916457A (ro)	1970-05-06
DE1953149A1 (de)	1970-05-06
DK128742B (da)	1974-06-24
AT295922B (de)	1972-01-25
IL33221A0 (en)	1969-12-31

Publication	Publication Date	Title
DE1953149A1 (de)	1970-05-06	Mikrobizide Mittel
EP0000333B1 (de)	1982-07-28	Derivate cyclischer Amine und diese enthaltende Fungizide
JPS6141353B2 (ro)	1986-09-13
DE68924662T2 (de)	1996-07-04	Beta-Phenoxynitril-Verbindungen.
IL31204A (en)	1972-09-28	Isoxazolyl carbamates and compositions containing them
DE2105174C3 (de)	1980-11-20	8-Oxychinolin- und 8-Oxychinaldinacrylate, Verfahren zu ihrer Herstellung und Mittel zur Bekämpfung von Mikroorganismen
DD229583A5 (de)	1985-11-13	Fungizides mittel
DE2118317A1 (ro)	1971-11-04
HU202521B (en)	1991-03-28	Fungicidal compositions comprising triazole oligoether derivatives as active ingredient and process for producing the active ingredient
DE3537290A1 (de)	1987-04-23	1,2,5-substituierte imidazolverbindungen, verfahren zu ihrer herstellung und ihre verwendung als wachstumsregulatoren
CA1227750A (en)	1987-10-06	Fungicidal compositions
HU193933B (en)	1987-12-28	Herbicide or plant growth stimulating agent comprising beta-cyclodextrin complex of benzolsulphonylurea derivative and process for preparing the active substances
US4602945A (en)	1986-07-29	Acaricidal ester of tricyclohexyl-tin hydroxide
US3697589A (en)	1972-10-10	N-(4-carboxy-benzylidene)amines
DE2044735C3 (de)	1979-09-27	Phenylharnstoffe, Verfahren zu ihrer Herstellung und diese enthaltende Schädlingsbekämpfungsmittel
EP0014999A1 (de)	1980-09-03	Optisch aktive Formen des 4-(3-(p-tert.-Butylphenyl)-2-methyl-propyl)-cis-2,6-dimethyl-morpholins und ihre Salze; Fungizide, die diese Verbindungen enthalten, und Verfahren zu ihrer Herstellung
PL152618B1 (en)	1991-01-31	Fungicide
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US3203855A (en)	1965-08-31	Method for combating fungi with 2-(2, 2, 2-trichloro-1-hydroxyethylamino) pyridine
GB2059418A (en)	1981-04-23	Pyroline derivatives and their use as acaricidal agents
US3836657A (en)	1974-09-17	Antifungal methods employing certain carbostyrils
DE2522474A1 (de)	1975-12-04	Fungicide mittel enthaltend n-alkylarcrylamide
US3751466A (en)	1973-08-07	N-benzylidene alkylamines
US3847947A (en)	1974-11-12	Quaternary thenyl phosphonium salts
US4931456A (en)	1990-06-05	Fungicidal oxime nicotinates