PL138494B1 - Pesticide and method of manufacture of novel substituted 1-phenyl-3-benzoyl-/thio/-ureas - Google Patents

Pesticide and method of manufacture of novel substituted 1-phenyl-3-benzoyl-/thio/-ureas Download PDF

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Publication number: PL138494B1
Authority: PL; Poland
Prior art keywords: hydrogen; halogen; formula; chlorine; atoms
Prior art date: 1983-03-19

Application number

PL1984246715A

Other languages

English (en)

Polish (pl)

Other versions

PL246715A1 (en

Original Assignee

Bayer 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.)

1983-03-19

Filing date

1984-03-16

Publication date

1986-09-30

1984-03-16 Application filed by Bayer Ag filed Critical Bayer Ag

1985-03-12 Publication of PL246715A1 publication Critical patent/PL246715A1/xx

1986-09-30 Publication of PL138494B1 publication Critical patent/PL138494B1/pl

Links

238000000034 method Methods 0.000 title claims description 13
238000004519 manufacturing process Methods 0.000 title description 4
239000000575 pesticide Substances 0.000 title description 4
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea group Chemical group NC(=S)N UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 title 1
239000000460 chlorine Substances 0.000 claims description 271
239000001257 hydrogen Substances 0.000 claims description 108
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229910052736 halogen Inorganic materials 0.000 claims description 63
150000002367 halogens Chemical group 0.000 claims description 60
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-1 benzoyl iso (thio) -cyanates Chemical class 0.000 claims description 43
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239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
230000001276 controlling effect Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000003651 drinking water Substances 0.000 description 1
235000020188 drinking water Nutrition 0.000 description 1
239000000428 dust Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
244000079386 endoparasite Species 0.000 description 1
230000012173 estrus Effects 0.000 description 1
229950005098 ethoxzolamide Drugs 0.000 description 1
125000004705 ethylthio group Chemical group C(C)S* 0.000 description 1
239000006260 foam Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
239000010903 husk Substances 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 1
150000002540 isothiocyanates Chemical class 0.000 description 1
230000001418 larval effect Effects 0.000 description 1
238000002386 leaching Methods 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
244000144972 livestock Species 0.000 description 1
239000004579 marble Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
244000005700 microbiome Species 0.000 description 1
239000003094 microcapsule Substances 0.000 description 1
239000008267 milk Substances 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
229920005615 natural polymer Polymers 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
125000003232 p-nitrobenzoyl group Chemical group [N+](=O)([O-])C1=CC=C(C(=O)*)C=C1 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
230000003071 parasitic effect Effects 0.000 description 1
239000006072 paste Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
229960003351 prussian blue Drugs 0.000 description 1
239000013225 prussian blue Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
239000007787 solid Substances 0.000 description 1
241000894007 species Species 0.000 description 1
235000020354 squash Nutrition 0.000 description 1
230000001954 sterilising effect Effects 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
ZWZVWGITAAIFPS-UHFFFAOYSA-N thiophosgene Chemical compound ClC(Cl)=S ZWZVWGITAAIFPS-UHFFFAOYSA-N 0.000 description 1
150000003606 tin compounds Chemical class 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
230000007306 turnover Effects 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- 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
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C273/00—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C273/02—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of urea, its salts, complexes or addition compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
- C07C275/48—Y being a hydrogen or a carbon atom
- C07C275/54—Y being a carbon atom of a six-membered aromatic ring, e.g. benzoylureas
- 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
- C07C323/10—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C323/18—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and singly-bound oxygen atoms bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
- C07C323/20—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and singly-bound oxygen atoms bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton with singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C335/04—Derivatives of thiourea
- C07C335/24—Derivatives of thiourea containing any of the groups, X being a hetero atom, Y being any atom
- C07C335/26—Y being a hydrogen or a carbon atom, e.g. benzoylthioureas

Landscapes

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

PL1984246715A 1983-03-19 1984-03-16 Pesticide and method of manufacture of novel substituted 1-phenyl-3-benzoyl-/thio/-ureas PL138494B1 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19833309987 DE3309987A1 (de)	1983-03-19	1983-03-19	Benzoylharnstoffe

Publications (2)

Publication Number	Publication Date
PL246715A1 PL246715A1 (en)	1985-03-12
PL138494B1 true PL138494B1 (en)	1986-09-30

Family

ID=6194024

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PL1984246715A PL138494B1 (en)	1983-03-19	1984-03-16	Pesticide and method of manufacture of novel substituted 1-phenyl-3-benzoyl-/thio/-ureas

Country Status (7)

Country	Link
JP (1)	JPS59176244A (cs)
KR (1)	KR840009081A (cs)
CS (1)	CS252814B2 (cs)
DE (1)	DE3309987A1 (cs)
HU (1)	HU193559B (cs)
PL (1)	PL138494B1 (cs)
ZA (1)	ZA841974B (cs)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3731561A1 (de) *	1987-09-19	1989-04-06	Basf Ag	N-benzoyl-n'-(2,3-dichlor-4-phenoxy)phenyl- harnstoffe

1983
- 1983-03-19 DE DE19833309987 patent/DE3309987A1/de not_active Withdrawn
1984
- 1984-03-15 CS CS841860A patent/CS252814B2/cs unknown
- 1984-03-16 JP JP59049401A patent/JPS59176244A/ja active Pending
- 1984-03-16 ZA ZA841974A patent/ZA841974B/xx unknown
- 1984-03-16 PL PL1984246715A patent/PL138494B1/pl unknown
- 1984-03-19 HU HU841074A patent/HU193559B/hu unknown
- 1984-03-19 KR KR1019840001398A patent/KR840009081A/ko not_active Withdrawn

Also Published As

Publication number	Publication date
DE3309987A1 (de)	1984-09-20
JPS59176244A (ja)	1984-10-05
KR840009081A (ko)	1984-12-24
PL246715A1 (en)	1985-03-12
ZA841974B (en)	1984-10-31
CS252814B2 (en)	1987-10-15
HU193559B (en)	1987-10-28

Publication	Publication Date	Title
US4533676A (en)	1985-08-06	2,5-Dihalogenobenzoyl-(thio)urea insecticides
US4711905A (en)	1987-12-08	2,4-dihalogenobenzoyl-(thio)urea insecticides
PL101199B1 (pl)	1978-12-30	Srodek owadobojczy
US4277499A (en)	1981-07-07	Combating insects with N-(substituted-phenyl)-N-(2-chloro-6-fluoro-benzoyl)-ureas
CA1110658A (en)	1981-10-13	Combating pests with n-(4-substituted-phenyl)-n'-(2- substituted-benzoyl)-thioureas
KR920001774B1 (ko)	1992-03-02	치환된 푸라잔의 제조방법
IE42472B1 (en)	1980-08-13	Benzoyl-ureido-diphenyl ethers and their use as insecticides
US4536587A (en)	1985-08-20	Combating pests with substituted benzoyl-(thio)ureas
US4103022A (en)	1978-07-25	Combating arthropods with 3-(2,2,4,4-tetrafluoro-benz-1,3-dioxin-6-yl)-1-(substituted benzoyl)-ureas
US4769481A (en)	1988-09-06	N-carbamoylaryl carboximidic acid esters, and their use as insecticides
US4342778A (en)	1982-08-03	Insecticidal (2,3-dihydro-2,2-dimethylbenzofuran-7-yloxy-N-methylcarbamoyl)-(N'-alkoxycarbamoyl)-sulphides
PL107560B1 (pl)	1980-02-29	Srodek owadobojczy
PL105423B1 (pl)	1979-10-31	Srodek owadobojczy
US4611003A (en)	1986-09-09	N-substituted benzoyl-N'-3,4-tetrafluoroethylenedioxy-urea pesticides
US4774260A (en)	1988-09-27	Novel benzoylurea pesticides
EP0123861B1 (de)	1988-04-20	Harnstoffderivate
PL101195B1 (pl)	1978-12-30	Srodek owadobojczy,roztoczobojczy i nicieniobojczy
PL115624B1 (en)	1981-04-30	Pesticide with insecticidal and acaricidal activity
JPH02270A (ja)	1990-01-05	（チオ）ベンゾイル尿素およびそれらの官能基誘導体、それらの製造方法、それらを含有する剤およびそれらの農薬としての使用方法
AU606474B2 (en)	1991-02-07	Furazanylureas
KR800000246B1 (ko)	1980-04-02	디페닐 에테르의 제조방법
HU193559B (en)	1987-10-28	Process for producing benzoyl-urea derivatives and pesticide co compositions containing them as active ingredients
JPH01168661A (ja)	1989-07-04	置換されたベンゾイル尿素及びチオ尿素
DE3341276A1 (de)	1985-05-23	Benzoylharnstoffe