JPS6011005B2 - 有害生物防除剤 - Google Patents

有害生物防除剤

Info

Publication number: JPS6011005B2
Authority: JP; Japan
Prior art keywords: group; methyl; dimethyl; formula; tables
Prior art date: 1972-05-10
Legal status (The legal status 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 status listed.): Expired

Application number

JP48052078A

Other languages

English (en)

Japanese (ja)

Other versions

JPS4954526A (de

Inventor

カラ− フリ−ドリツヒ

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Novartis AG

Original Assignee

Ciba Geigy 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.)

1972-05-10

Filing date

1973-05-10

Publication date

1985-03-22

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=27174895&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=JPS6011005(B2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1972-05-10 Priority claimed from CH701172A external-priority patent/CH566709A5/de

1972-09-29 Priority claimed from CH1425572A external-priority patent/CH578317A5/de

1973-03-29 Priority claimed from CH456773A external-priority patent/CH578825A5/de

1973-05-10 Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG

1974-05-27 Publication of JPS4954526A publication Critical patent/JPS4954526A/ja

1985-03-22 Publication of JPS6011005B2 publication Critical patent/JPS6011005B2/ja

Status Expired legal-status Critical Current

Links

241000607479 Yersinia pestis Species 0.000 title claims description 4
-1 cyclohexyloxycarbonyl group Chemical group 0.000 claims description 62
150000001875 compounds Chemical group 0.000 claims description 28
239000001257 hydrogen Substances 0.000 claims description 18
229910052739 hydrogen Inorganic materials 0.000 claims description 18
239000000126 substance Substances 0.000 claims description 17
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 12
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 9
239000000654 additive Substances 0.000 claims description 8
229910052736 halogen Inorganic materials 0.000 claims description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
239000003795 chemical substances by application Substances 0.000 claims description 6
125000004093 cyano group Chemical group *C#N 0.000 claims description 6
150000002367 halogens Chemical class 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 5
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 5
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 5
125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
229910052757 nitrogen Inorganic materials 0.000 claims description 4
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 3
125000002933 cyclohexyloxy group Chemical group C1(CCCCC1)O* 0.000 claims description 3
125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 3
125000000623 heterocyclic group Chemical group 0.000 claims description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
125000006678 phenoxycarbonyl group Chemical group 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
229910052717 sulfur Inorganic materials 0.000 claims description 2
125000004434 sulfur atom Chemical group 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims 3
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
125000006527 (C1-C5) alkyl group Chemical group 0.000 claims 1
239000004480 active ingredient Substances 0.000 description 53
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 42
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical class CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 38
239000000243 solution Substances 0.000 description 36
239000000203 mixture Substances 0.000 description 31
238000011156 evaluation Methods 0.000 description 18
239000002904 solvent Substances 0.000 description 16
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
125000004435 hydrogen atom Chemical group [H]* 0.000 description 13
239000008187 granular material Substances 0.000 description 12
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239000000843 powder Substances 0.000 description 11
230000000694 effects Effects 0.000 description 10
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229910052783 alkali metal Inorganic materials 0.000 description 9
239000010452 phosphate Substances 0.000 description 9
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229910052801 chlorine Inorganic materials 0.000 description 7
238000009472 formulation Methods 0.000 description 7
238000002844 melting Methods 0.000 description 7
230000008018 melting Effects 0.000 description 7
RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 7
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
WFDIJRYMOXRFFG-UHFFFAOYSA-N acetic acid anhydride Natural products CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
239000000460 chlorine Substances 0.000 description 6
239000002270 dispersing agent Substances 0.000 description 6
239000000839 emulsion Substances 0.000 description 6
150000002576 ketones Chemical class 0.000 description 6
238000000034 method Methods 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
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239000005995 Aluminium silicate Substances 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
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239000002253 acid Substances 0.000 description 5
235000012211 aluminium silicate Nutrition 0.000 description 5
239000012876 carrier material Substances 0.000 description 5
150000002191 fatty alcohols Chemical group 0.000 description 5
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 5
239000003960 organic solvent Substances 0.000 description 5
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
229910052938 sodium sulfate Inorganic materials 0.000 description 5
235000011152 sodium sulphate Nutrition 0.000 description 5
239000007787 solid Substances 0.000 description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
239000002202 Polyethylene glycol Substances 0.000 description 4
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
238000009835 boiling Methods 0.000 description 4
239000004202 carbamide Substances 0.000 description 4
239000007859 condensation product Substances 0.000 description 4
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 4
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 4
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 4
239000006072 paste Substances 0.000 description 4
229920001223 polyethylene glycol Polymers 0.000 description 4
229920000151 polyglycol Polymers 0.000 description 4
239000010695 polyglycol Substances 0.000 description 4
FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
235000012239 silicon dioxide Nutrition 0.000 description 4
239000008096 xylene Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
ZHLKXBJTJHRTTE-UHFFFAOYSA-N Chlorobenside Chemical compound C1=CC(Cl)=CC=C1CSC1=CC=C(Cl)C=C1 ZHLKXBJTJHRTTE-UHFFFAOYSA-N 0.000 description 3
241000254173 Coleoptera Species 0.000 description 3
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 3
241000196324 Embryophyta Species 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
241000257303 Hymenoptera Species 0.000 description 3
244000061456 Solanum tuberosum Species 0.000 description 3
235000002595 Solanum tuberosum Nutrition 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000000853 adhesive Substances 0.000 description 3
230000001070 adhesive effect Effects 0.000 description 3
150000001340 alkali metals Chemical class 0.000 description 3
239000008346 aqueous phase Substances 0.000 description 3
239000002585 base Substances 0.000 description 3
XSCHRSMBECNVNS-UHFFFAOYSA-N benzopyrazine Natural products N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 3
235000013339 cereals Nutrition 0.000 description 3
235000019993 champagne Nutrition 0.000 description 3
125000001309 chloro group Chemical group Cl* 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
238000001816 cooling Methods 0.000 description 3
239000000428 dust Substances 0.000 description 3
239000000463 material Substances 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000012071 phase Substances 0.000 description 3
125000005930 sec-butyloxycarbonyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 description 3
239000000741 silica gel Substances 0.000 description 3
229910002027 silica gel Inorganic materials 0.000 description 3
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 3
159000000000 sodium salts Chemical class 0.000 description 3
239000007921 spray Substances 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000000454 talc Substances 0.000 description 3
229910052623 talc Inorganic materials 0.000 description 3
235000012222 talc Nutrition 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 2
UHIDXDTXRPEJKK-UHFFFAOYSA-N 1-(4-benzylphenoxy)propan-2-one Chemical compound C1=CC(OCC(=O)C)=CC=C1CC1=CC=CC=C1 UHIDXDTXRPEJKK-UHFFFAOYSA-N 0.000 description 2
ZSBDGXGICLIJGD-UHFFFAOYSA-N 4-phenoxyphenol Chemical compound C1=CC(O)=CC=C1OC1=CC=CC=C1 ZSBDGXGICLIJGD-UHFFFAOYSA-N 0.000 description 2
241000256118 Aedes aegypti Species 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
STUSTWKEFDQFFZ-UHFFFAOYSA-N Chlordimeform Chemical compound CN(C)C=NC1=CC=C(Cl)C=C1C STUSTWKEFDQFFZ-UHFFFAOYSA-N 0.000 description 2
241001641896 Dermestes lardarius Species 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
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VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
240000008415 Lactuca sativa Species 0.000 description 2
235000003228 Lactuca sativa Nutrition 0.000 description 2
235000019738 Limestone Nutrition 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
240000002853 Nelumbo nucifera Species 0.000 description 2
235000006508 Nelumbo nucifera Nutrition 0.000 description 2
235000006510 Nelumbo pentapetala Nutrition 0.000 description 2
240000007594 Oryza sativa Species 0.000 description 2
235000007164 Oryza sativa Nutrition 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 2
DTAPQAJKAFRNJB-UHFFFAOYSA-N Promecarb Chemical compound CNC(=O)OC1=CC(C)=CC(C(C)C)=C1 DTAPQAJKAFRNJB-UHFFFAOYSA-N 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
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241001124072 Reduviidae Species 0.000 description 2
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CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
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239000013543 active substance Substances 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
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239000002518 antifoaming agent Substances 0.000 description 2
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125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
239000011575 calcium Substances 0.000 description 2
GTCAXTIRRLKXRU-UHFFFAOYSA-N carbamic acid methyl ester Natural products COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 description 2
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239000001913 cellulose Substances 0.000 description 2
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MJQBFSWPMMHVSM-UHFFFAOYSA-N chlorphthalim Chemical compound C1=CC(Cl)=CC=C1N1C(=O)C(CCCC2)=C2C1=O MJQBFSWPMMHVSM-UHFFFAOYSA-N 0.000 description 2
238000004587 chromatography analysis Methods 0.000 description 2
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150000002790 naphthalenes Chemical class 0.000 description 2
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125000000913 palmityl 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])C([H])([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 description 2
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RGCLLPNLLBQHPF-HJWRWDBZSA-N phosphamidon Chemical compound CCN(CC)C(=O)C(\Cl)=C(/C)OP(=O)(OC)OC RGCLLPNLLBQHPF-HJWRWDBZSA-N 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
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YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
229910052905 tridymite Inorganic materials 0.000 description 1
PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
244000045561 useful plants Species 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000002023 wood Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/511—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
- C07C45/515—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups the singly bound functional group being an acetalised, ketalised hemi-acetalised, or hemi-ketalised hydroxyl group
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/20—Unsaturated compounds containing keto groups bound to acyclic carbon atoms
- C07C49/255—Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing ether groups, groups, groups, or groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
- C07C59/66—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
- C07C59/68—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Pyridine Compounds (AREA)

JP48052078A 1972-05-10 1973-05-10 有害生物防除剤 Expired JPS6011005B2 (ja)

Applications Claiming Priority (6)

Application Number	Priority Date	Filing Date	Title
CH7011/72		1972-05-10
CH701172A CH566709A5 (en)	1972-05-10	1972-05-10	Phenyl-substd butenoic acid derivs - with insectidal activity
CH1425572A CH578317A5 (en)	1972-09-29	1972-09-29	Phenyl-substd butenoic acid derivs - with insectidal activity
CH14255/72		1972-09-29
CH456773A CH578825A5 (en)	1973-03-29	1973-03-29	Phenyl-substd butenoic acid derivs - with insectidal activity
CH4567/73		1973-03-29

Publications (2)

Publication Number	Publication Date
JPS4954526A JPS4954526A (de)	1974-05-27
JPS6011005B2 true JPS6011005B2 (ja)	1985-03-22

Family

ID=27174895

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP48052078A Expired JPS6011005B2 (ja)	1972-05-10	1973-05-10	有害生物防除剤

Country Status (18)

Country	Link
JP (1)	JPS6011005B2 (de)
AT (1)	AT328223B (de)
CA (1)	CA1055511A (de)
DD (1)	DD109315A5 (de)
DE (1)	DE2322853C3 (de)
DK (1)	DK134463B (de)
EG (1)	EG11425A (de)
ES (1)	ES414565A1 (de)
FI (1)	FI55986C (de)
FR (1)	FR2189368B1 (de)
GB (1)	GB1422181A (de)
HU (1)	HU168015B (de)
IL (1)	IL42156A (de)
IT (1)	IT994860B (de)
NL (1)	NL175813C (de)
OA (1)	OA04387A (de)
PH (1)	PH10001A (de)
SE (1)	SE402584B (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1479297A (en) *	1974-07-04	1977-07-13	Beecham Group Ltd	4-substituted butan-2-ones but-3-en-2-ones butan-2-ols and but-3-en-2-ols and pharmaceutical compositions containing them
CH609024A5 (en) *	1974-09-30	1979-02-15	Lafon Labor	Process for the preparation of new sulphur-containing diaryl and oxygen-containing diaryl compounds
GB2105715B (en) *	1981-08-07	1985-09-04	Ciba Geigy Ag	Herbicidal phenoxyphenylamino acid derivatives

1973
- 1973-04-16 FI FI1200/73A patent/FI55986C/fi active
- 1973-04-24 SE SE7305715A patent/SE402584B/xx unknown
- 1973-05-01 IL IL42156A patent/IL42156A/en unknown
- 1973-05-03 PH PH14599A patent/PH10001A/en unknown
- 1973-05-07 DE DE2322853A patent/DE2322853C3/de not_active Expired
- 1973-05-09 AT AT407773A patent/AT328223B/de not_active IP Right Cessation
- 1973-05-09 ES ES414565A patent/ES414565A1/es not_active Expired
- 1973-05-09 CA CA170,842A patent/CA1055511A/en not_active Expired
- 1973-05-09 DK DK256273AA patent/DK134463B/da unknown
- 1973-05-09 DD DD170727A patent/DD109315A5/xx unknown
- 1973-05-09 GB GB2221373A patent/GB1422181A/en not_active Expired
- 1973-05-09 EG EG170/73A patent/EG11425A/xx active
- 1973-05-09 IT IT23886/73A patent/IT994860B/it active
- 1973-05-09 FR FR7316675A patent/FR2189368B1/fr not_active Expired
- 1973-05-10 NL NLAANVRAGE7306547,A patent/NL175813C/xx not_active IP Right Cessation
- 1973-05-10 OA OA54907A patent/OA04387A/xx unknown
- 1973-05-10 JP JP48052078A patent/JPS6011005B2/ja not_active Expired
1974
- 1974-05-09 HU HUCI1371A patent/HU168015B/hu unknown

Also Published As

Publication number	Publication date
NL7306547A (de)	1973-11-13
GB1422181A (en)	1976-01-21
FR2189368B1 (de)	1978-01-06
IL42156A0 (en)	1973-07-30
DE2322853C3 (de)	1981-01-15
DE2322853A1 (de)	1973-11-29
AU5527273A (en)	1974-11-07
FI55986C (fi)	1979-11-12
OA04387A (fr)	1980-02-15
FR2189368A1 (de)	1974-01-25
NL175813B (nl)	1984-08-01
IT994860B (it)	1975-10-20
HU168015B (de)	1976-02-28
CA1055511A (en)	1979-05-29
DD109315A5 (de)	1974-11-05
JPS4954526A (de)	1974-05-27
AT328223B (de)	1976-03-10
SE402584B (sv)	1978-07-10
DE2322853B2 (de)	1980-05-08
PH10001A (en)	1976-07-13
DK134463B (da)	1976-11-15
FI55986B (fi)	1979-07-31
DK134463C (de)	1977-05-16
EG11425A (en)	1977-08-15
ES414565A1 (es)	1976-05-16
IL42156A (en)	1976-11-30
NL175813C (nl)	1985-01-02
ATA407773A (de)	1975-05-15

Publication	Publication Date	Title
CA1301169C (en)	1992-05-19	1,5-diphenylpyrazole-3-carboxylic acid derivatives for the protection of cultivated plants
JPS5844649B2 (ja)	1983-10-04	エ−テルユウドウタイノセイホウ
SI9300220A (sl)	1993-12-31	Fungicidni arilpirazoli
US4069344A (en)	1978-01-17	Insecticidal substituted phenyl derivatives
JPS6041041B2 (ja)	1985-09-13	有害生物防除剤及びその製法
EP0008645A1 (de)	1980-03-19	Alkoxyphenylpyrrolidone, Verfahren zu ihrer Herstellung und Arzneimittel auf Basis dieser Verbindungen
JPS6011011B2 (ja)	1985-03-22	有害生物防除剤及びその製造方法
US4670451A (en)	1987-06-02	Benzoxazolone-2 compounds and fungicidal use thereof
US4172146A (en)	1979-10-23	Substituted phenyl derivatives
DE2418343A1 (de)	1974-11-07	Phenyl-aralkyl-aether, -thioaether und -amine, verfahren zu ihrer herstellung und ihre verwendung
JP2553156B2 (ja)	1996-11-13	アリールピロール殺昆虫、殺ダニおよび殺線虫剤およびそれらの調製方法
US3941829A (en)	1976-03-02	N-phenyl-N'-carbophenoxy formamidines
DE2338819A1 (de)	1974-02-14	Schaedlingsbekaempfungsmittel
JPS6036403B2 (ja)	1985-08-20	有害生物防除剤及びその製造方法
CA1055511A (en)	1979-05-29	Substituted phenyl derivatives
US3998855A (en)	1976-12-21	Epoxyalkoxy substituted benzophenones
US3933945A (en)	1976-01-20	O-ethyl-S-(n)propyl-S-diallylcarbmoylmethyldithiophosphate
DE2312518A1 (de)	1973-09-20	Neue aryl-aether-derivate
US3932629A (en)	1976-01-13	Triazolyl phosphorus esters as pesticides
US3973010A (en)	1976-08-03	Insecticidal and acaricidal composition and method with triazolyl phosphoric esters acid
US4171371A (en)	1979-10-16	Diketones
US4056622A (en)	1977-11-01	N-sulfonyl-N-dihalophenylimidazolidinediones
US3991140A (en)	1976-11-09	O-ethyl-S-(n)-propyl-s-carbamoylalkyl dithiophosphates
JPS6140665B2 (de)	1986-09-10
US3954793A (en)	1976-05-04	1-(2-Propynyl)-1 H-indazole compounds