LU83725A1 - Composes organiques sulfures et leur utilisation comme acaricides,insecticides et/ou fongicides - Google Patents

Composes organiques sulfures et leur utilisation comme acaricides,insecticides et/ou fongicides Download PDF

Info

Publication number: LU83725A1
Authority: LU; Luxembourg
Prior art keywords: active ingredient; composition according; insecticide; acaricide; new
Prior art date: 1981-10-29

Application number

LU83725A

Other languages

English (en)

French (fr)

Inventor

Jean Marie De Muylder

Original Assignee

Seresci

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.)

1981-10-29

Filing date

1981-10-29

Publication date

1983-06-07

1981-10-29 Application filed by Seresci filed Critical Seresci

1981-10-29 Priority to LU83725A priority Critical patent/LU83725A1/fr

1982-10-18 Priority to AT82201292T priority patent/ATE17635T1/de

1982-10-18 Priority to EP82201292A priority patent/EP0078562B1/de

1982-10-18 Priority to DE8282201292T priority patent/DE3268870D1/de

1982-10-20 Priority to CA000413813A priority patent/CA1173747A/en

1982-10-25 Priority to AU89750/82A priority patent/AU8975082A/en

1983-06-07 Publication of LU83725A1 publication Critical patent/LU83725A1/fr

Links

239000000642 acaricide Substances 0.000 title claims description 39
239000000417 fungicide Substances 0.000 title claims description 39
239000002917 insecticide Substances 0.000 title claims description 39
150000002894 organic compounds Chemical class 0.000 title abstract description 3
239000000203 mixture Substances 0.000 claims abstract description 54
239000004480 active ingredient Substances 0.000 claims abstract description 50
230000000895 acaricidal effect Effects 0.000 claims abstract description 43
125000003438 dodecyl group Chemical group [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])* 0.000 claims abstract description 17
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 17
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 15
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims abstract description 11
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 4
230000000855 fungicidal effect Effects 0.000 claims description 45
-1 propyl radicals Chemical class 0.000 claims description 37
150000003254 radicals Chemical class 0.000 claims description 23
150000007970 thio esters Chemical class 0.000 claims description 17
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 claims description 12
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 12
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 11
150000001875 compounds Chemical class 0.000 claims description 10
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 8
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 7
VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Substances CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 7
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
239000007788 liquid Substances 0.000 claims description 4
125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
150000002898 organic sulfur compounds Chemical class 0.000 claims description 4
239000002453 shampoo Substances 0.000 claims description 4
RNYWZRLFWZWGAB-UHFFFAOYSA-N CC(C(OCCCCCCCC)=S)(C)C Chemical compound CC(C(OCCCCCCCC)=S)(C)C RNYWZRLFWZWGAB-UHFFFAOYSA-N 0.000 claims description 3
QJBMZXCVKOCGIE-UHFFFAOYSA-N CCCCCCCCOC(=S)CCCCCCC Chemical compound CCCCCCCCOC(=S)CCCCCCC QJBMZXCVKOCGIE-UHFFFAOYSA-N 0.000 claims description 3
ATPSGMNOXJMMJF-UHFFFAOYSA-N O-benzyl octanethioate Chemical compound C(CCCCCCC)(=S)OCC1=CC=CC=C1 ATPSGMNOXJMMJF-UHFFFAOYSA-N 0.000 claims description 3
239000002674 ointment Substances 0.000 claims description 3
FBRFRKHFCOMZBK-UHFFFAOYSA-N C(CCC)(=S)OCCCCCCCC Chemical compound C(CCC)(=S)OCCCCCCCC FBRFRKHFCOMZBK-UHFFFAOYSA-N 0.000 claims description 2
ZBEDKZSFTVRFAF-UHFFFAOYSA-N C(CCC)(=S)OCCCCCCCCCCCCCCCC Chemical compound C(CCC)(=S)OCCCCCCCCCCCCCCCC ZBEDKZSFTVRFAF-UHFFFAOYSA-N 0.000 claims description 2
RPPRAKZILXSTAF-UHFFFAOYSA-N C(CCCCCCCCCCC)OC(CCC)=S Chemical compound C(CCCCCCCCCCC)OC(CCC)=S RPPRAKZILXSTAF-UHFFFAOYSA-N 0.000 claims description 2
IDJYQSLXEGQESY-UHFFFAOYSA-N O-benzyl 2,2-dimethylpropanethioate Chemical compound C(C(C)(C)C)(=S)OCC1=CC=CC=C1 IDJYQSLXEGQESY-UHFFFAOYSA-N 0.000 claims description 2
MHEUJFLNACRFSW-UHFFFAOYSA-N O-dodecyl benzenecarbothioate Chemical compound C(C1=CC=CC=C1)(=S)OCCCCCCCCCCCC MHEUJFLNACRFSW-UHFFFAOYSA-N 0.000 claims description 2
WOHXSJKVJNXLFS-UHFFFAOYSA-N O-dodecyl octanethioate Chemical compound C(CCCCCCC)(=S)OCCCCCCCCCCCC WOHXSJKVJNXLFS-UHFFFAOYSA-N 0.000 claims description 2
OCBFFGCSTGGPSQ-UHFFFAOYSA-N [CH2]CC Chemical compound [CH2]CC OCBFFGCSTGGPSQ-UHFFFAOYSA-N 0.000 claims description 2
XEAATKLXMMFXDN-UHFFFAOYSA-N benzyl thiophene-2-carboxylate Chemical compound C=1C=CSC=1C(=O)OCC1=CC=CC=C1 XEAATKLXMMFXDN-UHFFFAOYSA-N 0.000 claims description 2
VUSZPSYSKPXZQL-UHFFFAOYSA-N butyl thiophene-2-carboxylate Chemical compound CCCCOC(=O)C1=CC=CS1 VUSZPSYSKPXZQL-UHFFFAOYSA-N 0.000 claims description 2
UZJAWMXDSAOZMR-UHFFFAOYSA-N o-benzyl 4-methoxybenzenecarbothioate Chemical compound C1=CC(OC)=CC=C1C(=S)OCC1=CC=CC=C1 UZJAWMXDSAOZMR-UHFFFAOYSA-N 0.000 claims description 2
VEGCUQREWHMYLG-UHFFFAOYSA-N o-benzyl butanethioate Chemical compound CCCC(=S)OCC1=CC=CC=C1 VEGCUQREWHMYLG-UHFFFAOYSA-N 0.000 claims description 2
MNMWCDPRBHPWAW-UHFFFAOYSA-N o-benzyl ethanethioate Chemical compound CC(=S)OCC1=CC=CC=C1 MNMWCDPRBHPWAW-UHFFFAOYSA-N 0.000 claims description 2
QXFWYSFHHKBVKG-UHFFFAOYSA-N o-cyclohexyl benzenecarbothioate Chemical compound C=1C=CC=CC=1C(=S)OC1CCCCC1 QXFWYSFHHKBVKG-UHFFFAOYSA-N 0.000 claims description 2
QPPJRFAUGVJUOY-UHFFFAOYSA-N o-dodecyl ethanethioate Chemical compound CCCCCCCCCCCCOC(C)=S QPPJRFAUGVJUOY-UHFFFAOYSA-N 0.000 claims description 2
QZSZNKPNTUZWQH-UHFFFAOYSA-N o-hexadecyl ethanethioate Chemical compound CCCCCCCCCCCCCCCCOC(C)=S QZSZNKPNTUZWQH-UHFFFAOYSA-N 0.000 claims description 2
PLOKVOUEDPRZPX-UHFFFAOYSA-N o-octyl ethanethioate Chemical compound CCCCCCCCOC(C)=S PLOKVOUEDPRZPX-UHFFFAOYSA-N 0.000 claims description 2
KXXZPIFZTPWOJJ-UHFFFAOYSA-N s-butyl benzenecarbothioate Chemical compound CCCCSC(=O)C1=CC=CC=C1 KXXZPIFZTPWOJJ-UHFFFAOYSA-N 0.000 claims description 2
230000000699 topical effect Effects 0.000 claims description 2
SXPUVBFQXJHYNS-UHFFFAOYSA-N α-furil Chemical group C=1C=COC=1C(=O)C(=O)C1=CC=CO1 SXPUVBFQXJHYNS-UHFFFAOYSA-N 0.000 claims description 2
230000000749 insecticidal effect Effects 0.000 claims 10
XDMPMKPZZNWXQP-UHFFFAOYSA-N O-hexadecyl 2-methylpropanethioate Chemical compound C(C(C)C)(=S)OCCCCCCCCCCCCCCCC XDMPMKPZZNWXQP-UHFFFAOYSA-N 0.000 claims 1
PYZDYCGDZMYSJQ-UHFFFAOYSA-N dodecyl thiophene-2-carboxylate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=CS1 PYZDYCGDZMYSJQ-UHFFFAOYSA-N 0.000 claims 1
WFBCZINRNWESPH-UHFFFAOYSA-N o-benzyl 2-methylpropanethioate Chemical compound CC(C)C(=S)OCC1=CC=CC=C1 WFBCZINRNWESPH-UHFFFAOYSA-N 0.000 claims 1
XFZZQJMBWJMTED-UHFFFAOYSA-N octyl thiophene-2-carboxylate Chemical compound CCCCCCCCOC(=O)C1=CC=CS1 XFZZQJMBWJMTED-UHFFFAOYSA-N 0.000 claims 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract description 4
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract description 2
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 2
239000005864 Sulphur Substances 0.000 abstract 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
238000009835 boiling Methods 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
238000000034 method Methods 0.000 description 3
239000007921 spray Substances 0.000 description 3
239000011593 sulfur Substances 0.000 description 3
229910052717 sulfur Inorganic materials 0.000 description 3
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
241000238876 Acari Species 0.000 description 2
206010063409 Acarodermatitis Diseases 0.000 description 2
241000447727 Scabies Species 0.000 description 2
230000001174 ascending effect Effects 0.000 description 2
238000004821 distillation Methods 0.000 description 2
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
238000001953 recrystallisation Methods 0.000 description 2
208000005687 scabies Diseases 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
241001474033 Acar Species 0.000 description 1
241001124076 Aphididae Species 0.000 description 1
241000239290 Araneae Species 0.000 description 1
241000283690 Bos taurus Species 0.000 description 1
241000282472 Canis lupus familiaris Species 0.000 description 1
241000359266 Chorioptes Species 0.000 description 1
229920000219 Ethylene vinyl alcohol Polymers 0.000 description 1
241000282326 Felis catus Species 0.000 description 1
241000233866 Fungi Species 0.000 description 1
241000238631 Hexapoda Species 0.000 description 1
239000004166 Lanolin Substances 0.000 description 1
241001480037 Microsporum Species 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000790252 Otodectes cynotis Species 0.000 description 1
239000005662 Paraffin oil Substances 0.000 description 1
241001674048 Phthiraptera Species 0.000 description 1
241000509416 Sarcoptes Species 0.000 description 1
241000258242 Siphonaptera Species 0.000 description 1
241000282887 Suidae Species 0.000 description 1
208000002474 Tinea Diseases 0.000 description 1
241000893966 Trichophyton verrucosum Species 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 description 1
229960000541 cetyl alcohol Drugs 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
239000003814 drug Substances 0.000 description 1
235000013601 eggs Nutrition 0.000 description 1
ALPIESLRVWNLAX-UHFFFAOYSA-N hexane-1,1-dithiol Chemical compound CCCCCC(S)S ALPIESLRVWNLAX-UHFFFAOYSA-N 0.000 description 1
229940039717 lanolin Drugs 0.000 description 1
235000019388 lanolin Nutrition 0.000 description 1
208000028454 lice infestation Diseases 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
229940056211 paraffin Drugs 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
150000003573 thiols Chemical class 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three 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
- C07D307/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/02—Saturated carboxylic acids or thio analogues thereof; Derivatives thereof
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group, wherein Cn means a carbon skeleton not containing a ring; Thio analogues thereof
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C327/00—Thiocarboxylic acids

Landscapes

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

LU83725A 1981-10-29 1981-10-29 Composes organiques sulfures et leur utilisation comme acaricides,insecticides et/ou fongicides LU83725A1 (fr)

Priority Applications (6)

Application Number	Priority Date	Filing Date	Title
LU83725A LU83725A1 (fr)	1981-10-29	1981-10-29	Composes organiques sulfures et leur utilisation comme acaricides,insecticides et/ou fongicides
AT82201292T ATE17635T1 (de)	1981-10-29	1982-10-18	Akarizide zusammensetzungen.
EP82201292A EP0078562B1 (de)	1981-10-29	1982-10-18	Akarizide Zusammensetzungen
DE8282201292T DE3268870D1 (de)	1981-10-29	1982-10-18	Acaricidal compositions
CA000413813A CA1173747A (en)	1981-10-29	1982-10-20	Acaricidal compositions
AU89750/82A AU8975082A (en)	1981-10-29	1982-10-25	Sulfur acaricidal compositions

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
LU83725		1981-10-29
LU83725A LU83725A1 (fr)	1981-10-29	1981-10-29	Composes organiques sulfures et leur utilisation comme acaricides,insecticides et/ou fongicides

Publications (1)

Publication Number	Publication Date
LU83725A1 true LU83725A1 (fr)	1983-06-07

Family

ID=19729753

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU83725A LU83725A1 (fr)	1981-10-29	1981-10-29	Composes organiques sulfures et leur utilisation comme acaricides,insecticides et/ou fongicides

Country Status (6)

Country	Link
EP (1)	EP0078562B1 (de)
AT (1)	ATE17635T1 (de)
AU (1)	AU8975082A (de)
CA (1)	CA1173747A (de)
DE (1)	DE3268870D1 (de)
LU (1)	LU83725A1 (de)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0472497A1 (de) *	1990-08-21	1992-02-26	Ciba-Geigy Ag	Thiobuttersäurederivate
EP1841318A1 (de) *	2005-01-26	2007-10-10	Merial Ltd.	Pestizidisch substituierte thioether

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2259869A (en) *	1939-09-30	1941-10-21	Shell Dev	Insecticide and repellent
BE603541A (de) *	1960-05-09
DE1793480A1 (de) *	1968-09-24	1972-02-24	Basf Ag	Fungizid
GB1501501A (en) *	1975-01-02	1978-02-15	Realisations Scient Soc Et	Acaricidal and ovicidal compositions
US4095970A (en) *	1976-06-16	1978-06-20	Stauffer Chemical Company	2,6-Dichlorothiolbenzoates and use thereof as plant growth regulators
GB1594962A (en) *	1978-02-02	1981-08-05	Shell Int Research	Pesticidal benzyl thio-carboxylate derivatives

1981
- 1981-10-29 LU LU83725A patent/LU83725A1/fr unknown
1982
- 1982-10-18 DE DE8282201292T patent/DE3268870D1/de not_active Expired
- 1982-10-18 AT AT82201292T patent/ATE17635T1/de not_active IP Right Cessation
- 1982-10-18 EP EP82201292A patent/EP0078562B1/de not_active Expired
- 1982-10-20 CA CA000413813A patent/CA1173747A/en not_active Expired
- 1982-10-25 AU AU89750/82A patent/AU8975082A/en not_active Abandoned

Also Published As

Publication number	Publication date
EP0078562B1 (de)	1986-01-29
CA1173747A (en)	1984-09-04
ATE17635T1 (de)	1986-02-15
EP0078562A1 (de)	1983-05-11
DE3268870D1 (de)	1986-03-13
AU8975082A (en)	1983-05-05

Publication	Publication Date	Title
CA2098122C (en)	2003-09-23	Anti-atherosclerotic aryl compounds
FR2465720A1 (fr)	1981-03-27	Phenoxyphenylisothiourees, procede pour leur preparation et leur application dans la lutte antiparasitaire ainsi que phenoxyphenylthiourees comme produits intermediaires pour la preparation des phenoxyphenylisothiourees ainsi que leur application dans la lutte antiparasitaire
FR2492376A1 (fr)	1982-04-23	Polymethylene-4,5 isothiazoline-4 ones-3, leur procede de preparation et leurs utilisation comme agents bactericides et fongicides
FR2490636A1 (fr)	1982-03-26	Derives de l'acide carbamique, leur preparation et produits pesticides en contenant
EP0480795A1 (de)	1992-04-15	Benzofuranderivate, ein Verfahren zu ihrer Herstellung, neue dadurch erhaltene Zwischenverbindungen, sowie ihre Anwendung als Pestizide
LU83725A1 (fr)	1983-06-07	Composes organiques sulfures et leur utilisation comme acaricides,insecticides et/ou fongicides
FR2568749A1 (fr)	1986-02-14	Composition a base d'un derive de thiolcarbamate, procede pour prolonger l'action des herbicides et compositions herbicides ayant une action prolongee
EP0489660A1 (de)	1992-06-10	Anwendung von Thiazolylalkoxyacrylaten in der Herstellung von Insektiziden und/oder Akanizide-Zusammensetzungen
FR2434148A1 (fr)	1980-03-21	Compositions presentant des proprietes de regulation de la croissance des plantes et des proprietes insecticides
US4128581A (en)	1978-12-05	Ketoxime carbamates
CH616314A5 (de)	1980-03-31
EP0342105A1 (de)	1989-11-15	2-Adamantyl-3-isothyazolin-4-one-Derivate, Verfahren zu ihrer Herstellung und ihre Anwendung als Bakterizide und Fungizide
CH660179A5 (fr)	1987-03-31	Derives de 1-phenoxy(phenylthio)-4-arylalkynyloxy-benzene pourvus d'une activite acaricide et d'une activite hormonale juvenile.
FR2572400A1 (fr)	1986-05-02	Insecticides de la pyrazoline
EP0002219B1 (de)	1980-12-10	Arzneimittel mit schwefelhaltigen Estern und Verfahren zu ihrer Herstellung
US4028413A (en)	1977-06-07	Ketoxime carbamates
EP0135510B1 (de)	1986-08-20	Halogen-benzophenon-oxim-derivate enthaltende arzneimittel
EP0014167B1 (de)	1982-06-30	Anilin-Derivate mit pilztötender Wirkung und Verfahren zu ihrer Herstellung
US5037991A (en)	1991-08-06	Novel substituted aromatic compounds
CA1220220A (fr)	1987-04-07	Oligomeres anioniques polythioalcanecarboxyliques, leur utilisation et nouveau procede de preparation
FR2524466A1 (fr)	1983-10-07	Composes heterocycliques azotes, leur preparation et produits fongicides en contenant
US3932471A (en)	1976-01-13	Azide
BE888179A (fr)	1981-09-30	Phenoxyphenylisothiourees, procede pour leur preparation et leur application dans la lutte antiparasitaire ainsi que phenoxyphenylthiourees comme produits intermediaires pour la preparation des phenoxyphenyliqothiourees ainsi que leur application dans la lutte antiparatitaire
US3884962A (en)	1975-05-20	Phenylcarbamates
EP0583198A1 (de)	1994-02-16	Imidazole Derivate, Verfahren zur deren Herstellung und deren Verwendung als Pestizid