CH622407A5 - Pesticidal composition containing organostannic compounds - Google Patents

Pesticidal composition containing organostannic compounds Download PDF

Info

Publication number: CH622407A5
Authority: CH; Switzerland
Prior art keywords: formula; composition according; radical; sucrose; cho
Prior art date: 1976-03-26

Application number

CH381677A

Other languages

English (en)

French (fr)

Inventor

Robert Clive Poller

Ann Parkin

Original Assignee

Research Corp

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.)

1976-03-26

Filing date

1977-03-25

Publication date

1981-04-15

1977-03-25 Application filed by Research Corp filed Critical Research Corp

1981-04-15 Publication of CH622407A5 publication Critical patent/CH622407A5/fr

Links

150000001875 compounds Chemical class 0.000 title claims description 67
239000000203 mixture Substances 0.000 title claims description 28
230000000361 pesticidal effect Effects 0.000 title description 2
-1 alkyl radical Chemical class 0.000 claims description 31
229930006000 Sucrose Natural products 0.000 claims description 25
239000005720 sucrose Substances 0.000 claims description 25
150000003254 radicals Chemical class 0.000 claims description 23
229910052718 tin Inorganic materials 0.000 claims description 23
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 19
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical group [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 19
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 15
150000003445 sucroses Chemical class 0.000 claims description 15
229910052799 carbon Inorganic materials 0.000 claims description 12
125000004432 carbon atom Chemical group C* 0.000 claims description 11
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 5
230000000895 acaricidal effect Effects 0.000 claims description 5
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 5
HSFWRNGVRCDJHI-UHFFFAOYSA-N Acetylene Chemical compound C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 4
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 4
125000005843 halogen group Chemical group 0.000 claims description 4
239000005977 Ethylene Substances 0.000 claims description 3
239000000642 acaricide Substances 0.000 claims description 3
150000005840 aryl radicals Chemical class 0.000 claims description 3
229910052801 chlorine Inorganic materials 0.000 claims description 3
125000000185 sucrose group Chemical group 0.000 claims description 3
YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical group [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
239000011780 sodium chloride Substances 0.000 claims description 2
229910052717 sulfur Inorganic materials 0.000 claims description 2
125000004434 sulfur atom Chemical group 0.000 claims description 2
229960004793 sucrose Drugs 0.000 claims 6
125000004429 atom Chemical group 0.000 claims 2
WPWHSFAFEBZWBB-UHFFFAOYSA-N 1-butyl radical Chemical group [CH2]CCC WPWHSFAFEBZWBB-UHFFFAOYSA-N 0.000 claims 1
125000001309 chloro group Chemical group Cl* 0.000 claims 1
235000013681 dietary sucrose Nutrition 0.000 claims 1
239000000575 pesticide Substances 0.000 claims 1
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 24
238000006243 chemical reaction Methods 0.000 description 10
238000004458 analytical method Methods 0.000 description 9
230000000694 effects Effects 0.000 description 8
150000002148 esters Chemical class 0.000 description 8
238000002329 infrared spectrum Methods 0.000 description 8
241000233866 Fungi Species 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 6
150000001721 carbon Chemical group 0.000 description 6
230000000855 fungicidal effect Effects 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
230000003115 biocidal effect Effects 0.000 description 5
239000000839 emulsion Substances 0.000 description 5
239000003973 paint Substances 0.000 description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
230000000844 anti-bacterial effect Effects 0.000 description 4
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000003139 biocide Substances 0.000 description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
229910052794 bromium Inorganic materials 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
229920001817 Agar Polymers 0.000 description 2
241000239290 Araneae Species 0.000 description 2
241000223651 Aureobasidium Species 0.000 description 2
241000079253 Byssochlamys spectabilis Species 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
241001149956 Cladosporium herbarum Species 0.000 description 2
241000371621 Stemphylium Species 0.000 description 2
241001454293 Tetranychus urticae Species 0.000 description 2
241000196252 Ulva Species 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
239000008272 agar Substances 0.000 description 2
230000002353 algacidal effect Effects 0.000 description 2
230000003373 anti-fouling effect Effects 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
229910000365 copper sulfate Inorganic materials 0.000 description 2
ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
230000002363 herbicidal effect Effects 0.000 description 2
238000000034 method Methods 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
BUYMVQAILCEWRR-UHFFFAOYSA-N naled Chemical compound COP(=O)(OC)OC(Br)C(Cl)(Cl)Br BUYMVQAILCEWRR-UHFFFAOYSA-N 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
229910000027 potassium carbonate Inorganic materials 0.000 description 2
238000000518 rheometry Methods 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 description 2
238000004448 titration Methods 0.000 description 2
DFNPRTKVCGZMMC-UHFFFAOYSA-M tributyl(fluoro)stannane Chemical compound CCCC[Sn](F)(CCCC)CCCC DFNPRTKVCGZMMC-UHFFFAOYSA-M 0.000 description 2
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 description 1
241000238876 Acari Species 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
241000251468 Actinopterygii Species 0.000 description 1
241000228197 Aspergillus flavus Species 0.000 description 1
241000203233 Aspergillus versicolor Species 0.000 description 1
235000007320 Avena fatua Nutrition 0.000 description 1
244000075850 Avena orientalis Species 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
241001474374 Blennius Species 0.000 description 1
241000195493 Cryptophyta Species 0.000 description 1
241000223208 Curvularia Species 0.000 description 1
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
241000588724 Escherichia coli Species 0.000 description 1
241000223221 Fusarium oxysporum Species 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
241000192041 Micrococcus Species 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
241000589597 Paracoccus denitrificans Species 0.000 description 1
241000791947 Paradendryphiella salina Species 0.000 description 1
241000228143 Penicillium Species 0.000 description 1
241001123663 Penicillium expansum Species 0.000 description 1
241000893212 Pestalotia Species 0.000 description 1
241001193612 Phoma violacea Species 0.000 description 1
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
241000235070 Saccharomyces Species 0.000 description 1
241001279364 Stachybotrys chartarum Species 0.000 description 1
241001540751 Talaromyces ruber Species 0.000 description 1
241000223261 Trichoderma viride Species 0.000 description 1
235000005373 Uvularia sessilifolia Nutrition 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000013543 active substance Substances 0.000 description 1
239000003513 alkali Substances 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
229940126214 compound 3 Drugs 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
239000006787 czapek-dox agar Substances 0.000 description 1
230000007547 defect Effects 0.000 description 1
238000010586 diagram Methods 0.000 description 1
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
235000013601 eggs Nutrition 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000000605 extraction Methods 0.000 description 1
BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 description 1
230000035784 germination Effects 0.000 description 1
239000011521 glass Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
231100000086 high toxicity Toxicity 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
238000007654 immersion Methods 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
238000011534 incubation Methods 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
231100001231 less toxic Toxicity 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000009630 liquid culture Methods 0.000 description 1
230000007774 longterm Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
YLGXILFCIXHCMC-JHGZEJCSSA-N methyl cellulose Chemical compound COC1C(OC)C(OC)C(COC)O[C@H]1O[C@H]1C(OC)C(OC)C(OC)OC1COC YLGXILFCIXHCMC-JHGZEJCSSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
150000002895 organic esters Chemical class 0.000 description 1
230000008520 organization Effects 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
238000010422 painting Methods 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
239000000049 pigment Substances 0.000 description 1
235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
229920000053 polysorbate 80 Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000004321 preservation Methods 0.000 description 1
238000000746 purification Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000013535 sea water Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000002689 soil Substances 0.000 description 1
230000004763 spore germination Effects 0.000 description 1
238000005507 spraying Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
150000003890 succinate salts Chemical class 0.000 description 1
229940014800 succinic anhydride Drugs 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical class C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
150000003606 tin compounds Chemical class 0.000 description 1
MUHFQLVFMFDJOK-UHFFFAOYSA-N triphenyl(triphenylstannyloxy)stannane Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)O[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 MUHFQLVFMFDJOK-UHFFFAOYSA-N 0.000 description 1
238000005406 washing Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H23/00—Compounds containing boron, silicon or a metal, e.g. chelates or vitamin B12

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Biochemistry (AREA)
Biotechnology (AREA)
General Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Molecular Biology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

CH381677A 1976-03-26 1977-03-25 Pesticidal composition containing organostannic compounds CH622407A5 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB1216876A GB1541055A (en)	1976-03-26	1976-03-26	Organotin compounds

Publications (1)

Publication Number	Publication Date
CH622407A5 true CH622407A5 (en)	1981-04-15

Family

ID=9999598

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH381677A CH622407A5 (en)	1976-03-26	1977-03-25	Pesticidal composition containing organostannic compounds

Country Status (9)

Country	Link
JP (1)	JPS52144630A (it)
BE (1)	BE852536A (it)
CA (1)	CA1065311A (it)
CH (1)	CH622407A5 (it)
DE (1)	DE2713585A1 (it)
FR (1)	FR2345462A1 (it)
GB (1)	GB1541055A (it)
IT (1)	IT1075679B (it)
NL (1)	NL7703085A (it)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FI73693C (fi) *	1983-02-22	1987-11-09	Schering Ag	Triorganotenn-acetylsalicylat och dessa innehaollande biocida aemnen.
AUPN029994A0 (en) *	1994-12-23	1995-01-27	Ici Australia Operations Proprietary Limited	Alkypolysaccharide derivatives & compositions

1976
- 1976-03-26 GB GB1216876A patent/GB1541055A/en not_active Expired
1977
- 1977-03-16 BE BE175844A patent/BE852536A/xx unknown
- 1977-03-22 NL NL7703085A patent/NL7703085A/xx not_active Application Discontinuation
- 1977-03-25 FR FR7709066A patent/FR2345462A1/fr active Granted
- 1977-03-25 CH CH381677A patent/CH622407A5/fr not_active IP Right Cessation
- 1977-03-25 IT IT2171677A patent/IT1075679B/it active
- 1977-03-26 JP JP3391377A patent/JPS52144630A/ja active Pending
- 1977-03-28 DE DE19772713585 patent/DE2713585A1/de not_active Withdrawn
- 1977-03-28 CA CA274,829A patent/CA1065311A/en not_active Expired

Also Published As

Publication number	Publication date
JPS52144630A (en)	1977-12-02
CA1065311A (en)	1979-10-30
FR2345462A1 (fr)	1977-10-21
BE852536A (fr)	1977-07-18
IT1075679B (it)	1985-04-22
FR2345462B3 (it)	1980-02-15
GB1541055A (en)	1979-02-21
DE2713585A1 (de)	1977-10-06
NL7703085A (nl)	1977-09-28

Legal Events

Date	Code	Title	Description
1983-11-30	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
CA1050558A (en)	1979-03-13	N-(substituted phenyl)-n-furanoyl-alanine methyl esters and their use in fungicidal compositions and methods
SU1083895A3 (ru)	1984-03-30	Фунгицидна композици
EP0378953B1 (fr)	1996-06-05	Benzylidène azolylméthylecycloalcane et utilisation comme fongicide
EP0151084A2 (fr)	1985-08-07	Fongicides à groupes triazole et oligoéther
CH622407A5 (en)	1981-04-15	Pesticidal composition containing organostannic compounds
JPH01305064A (ja)	1989-12-08	２―フエニルスルフイニル―ニトロ―ピリジン類
EP0246982B1 (fr)	1993-02-03	Composés à groupements triazole ou imidazole et tétrahydrofurane utilisation de cuex-ci à titre de fongicides et procédés de préparation
CH640700A5 (fr)	1984-01-31	Composes et composition fongicide.
BE886127A (fr)	1981-05-13	Nouveaux derives de l'imidazole, leur preparation et leur application comme agents fongicides
EP0318400A1 (fr)	1989-05-31	Composés à groupements triazole, utilisation de ceux-ci à titre de fongicides et procédés de préparation
EP0850239A1 (en)	1998-07-01	Pesticidal compounds
Paulus	1988	Developments in microbicides for the protection of materials
SU649295A3 (ru)	1979-02-25	Инсектицидное средство
FR2519635A1 (fr)	1983-07-18	Imidazolyl-propiononitriles, procede pour les preparer et produits biocides contenant de tels composes
CH618679A5 (it)	1980-08-15
EP0249567A2 (fr)	1987-12-16	Dérivés propargyloxybenzènes, leur préparation et compositions fongicides les contenant
CH633775A5 (fr)	1982-12-31	N-(2-methyl-1-naphtyl)maleimide, utile comme biocide, et son procede de preparation.
CH639643A5 (en)	1983-11-30	Pesticides
JPH11502503A (ja)	1999-03-02	置換チアジアゾール類、それらを含有する組成物並びに抗微生物剤及び海産生物による汚染に対する防止剤としてのそれらの使用
WO2016042280A1 (fr)	2016-03-24	Conjugues d'acide amine-pyridine/pyridinium et leurs utilisations en tant qu'agents biocides
JPS6143156A (ja)	1986-03-01	Ｎ，ｎ‐ジエチル‐ｎ′‐アリール‐ｎ′‐（ジクロロフルオロメチルチオ）‐スルフアミド及びその製造方法並びに使用
JPH04225950A (ja)	1992-08-14	アルキレンビスジチオカーバメート中のｅｔｕ含量の減少及び抑制
CN117402121A (zh)	2024-01-16	一种含三唑啉酮结构的化合物及其制备方法和应用
JPS58113107A (ja)	1983-07-05	除草剤
EP0077281A1 (fr)	1983-04-20	Nouveaux fongicides homologués des N-phényl alaninates et leur procédé de préparation et leur application