CS196301B2 - Fungicide - Google Patents

Fungicide Download PDF

Info

Publication number: CS196301B2
Authority: CS; Czechoslovakia
Prior art keywords: active ingredient; composition according; compound; thio; plants
Prior art date: 1975-02-05

Application number

CS76642A

Other languages

Czech (cs)

English (en)

Inventor

Croix Guy La

Jean-Claude Debourge

Jacques Ducret

Original Assignee

Philagro Sa

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.)

1975-02-05

Filing date

1976-02-02

Publication date

1980-03-31

1976-02-02 Application filed by Philagro Sa filed Critical Philagro Sa

1980-03-31 Publication of CS196301B2 publication Critical patent/CS196301B2/cs

Links

230000000855 fungicidal effect Effects 0.000 title claims abstract description 9
239000000417 fungicide Substances 0.000 title abstract description 4
150000001875 compounds Chemical class 0.000 claims abstract description 29
239000000203 mixture Substances 0.000 claims abstract description 20
125000000217 alkyl group Chemical group 0.000 claims abstract description 4
125000001188 haloalkyl group Chemical group 0.000 claims abstract description 3
125000001624 naphthyl group Chemical group 0.000 claims abstract description 3
239000004480 active ingredient Substances 0.000 claims description 17
229910052739 hydrogen Inorganic materials 0.000 claims description 12
239000013543 active substance Substances 0.000 claims description 5
125000004432 carbon atom Chemical group C* 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
208000031888 Mycoses Diseases 0.000 claims 1
KGQCLZJFUIPDGS-UHFFFAOYSA-N dioxaphospholane Chemical compound C1CPOO1 KGQCLZJFUIPDGS-UHFFFAOYSA-N 0.000 claims 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
239000001257 hydrogen Substances 0.000 claims 1
125000004122 cyclic group Chemical group 0.000 abstract description 4
239000004615 ingredient Substances 0.000 abstract description 2
239000003960 organic solvent Substances 0.000 abstract description 2
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
125000003545 alkoxy group Chemical group 0.000 abstract 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
125000001475 halogen functional group Chemical group 0.000 abstract 1
241000196324 Embryophyta Species 0.000 description 17
229910052698 phosphorus Inorganic materials 0.000 description 12
229910052799 carbon Inorganic materials 0.000 description 11
239000000725 suspension Substances 0.000 description 10
238000002474 experimental method Methods 0.000 description 9
239000000126 substance Substances 0.000 description 8
241000233866 Fungi Species 0.000 description 7
239000004563 wettable powder Substances 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
229910052717 sulfur Inorganic materials 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 5
208000015181 infectious disease Diseases 0.000 description 5
-1 sodium alkylarylsulfonate Chemical class 0.000 description 5
238000005507 spraying Methods 0.000 description 5
230000009885 systemic effect Effects 0.000 description 5
239000007900 aqueous suspension Substances 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
244000053095 fungal pathogen Species 0.000 description 4
239000000080 wetting agent Substances 0.000 description 4
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
244000046052 Phaseolus vulgaris Species 0.000 description 3
235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000011575 calcium Substances 0.000 description 3
229910052791 calcium Inorganic materials 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
239000000945 filler Substances 0.000 description 3
230000035784 germination Effects 0.000 description 3
238000001727 in vivo Methods 0.000 description 3
230000001939 inductive effect Effects 0.000 description 3
238000000034 method Methods 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
241000123650 Botrytis cinerea Species 0.000 description 2
241000222235 Colletotrichum orbiculare Species 0.000 description 2
240000008067 Cucumis sativus Species 0.000 description 2
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
241000223221 Fusarium oxysporum Species 0.000 description 2
241000233626 Plasmopara Species 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
241000233639 Pythium Species 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
240000006365 Vitis vinifera Species 0.000 description 2
235000014787 Vitis vinifera Nutrition 0.000 description 2
YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 2
FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
238000009835 boiling Methods 0.000 description 2
229940125904 compound 1 Drugs 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000012153 distilled water Substances 0.000 description 2
239000004495 emulsifiable concentrate Substances 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
238000009472 formulation Methods 0.000 description 2
239000011521 glass Substances 0.000 description 2
229910000037 hydrogen sulfide Inorganic materials 0.000 description 2
238000000338 in vitro Methods 0.000 description 2
239000007788 liquid Substances 0.000 description 2
230000003071 parasitic effect Effects 0.000 description 2
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
230000003449 preventive effect Effects 0.000 description 2
239000011734 sodium Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000003381 stabilizer Substances 0.000 description 2
LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 description 1
JQSWMDZTSSQVBX-UHFFFAOYSA-N 1-(oxomethylidene)-3-phenylthiourea Chemical class O=C=NC(=S)NC1=CC=CC=C1 JQSWMDZTSSQVBX-UHFFFAOYSA-N 0.000 description 1
SPAMRUYRVYMHPV-UHFFFAOYSA-N 3a,4,5,7a-tetrahydroisoindole-1,3-dione Chemical class C1=CCCC2C(=O)NC(=O)C21 SPAMRUYRVYMHPV-UHFFFAOYSA-N 0.000 description 1
XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 1
229920001817 Agar Polymers 0.000 description 1
244000291564 Allium cepa Species 0.000 description 1
235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
244000099147 Ananas comosus Species 0.000 description 1
235000007119 Ananas comosus Nutrition 0.000 description 1
241000233685 Bremia lactucae Species 0.000 description 1
235000002566 Capsicum Nutrition 0.000 description 1
240000004160 Capsicum annuum Species 0.000 description 1
235000008534 Capsicum annuum var annuum Nutrition 0.000 description 1
239000005745 Captan Substances 0.000 description 1
241001620052 Cercosporella Species 0.000 description 1
241000207199 Citrus Species 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical class [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 description 1
241000219112 Cucumis Species 0.000 description 1
235000015510 Cucumis melo subsp melo Nutrition 0.000 description 1
241000371644 Curvularia ravenelii Species 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
240000009088 Fragaria x ananassa Species 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
235000008694 Humulus lupulus Nutrition 0.000 description 1
235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
239000005802 Mancozeb Substances 0.000 description 1
244000061176 Nicotiana tabacum Species 0.000 description 1
235000002637 Nicotiana tabacum Nutrition 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
241001223281 Peronospora Species 0.000 description 1
241000169463 Peronospora sp. Species 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
241000233614 Phytophthora Species 0.000 description 1
241001149949 Phytophthora cactorum Species 0.000 description 1
241000233616 Phytophthora capsici Species 0.000 description 1
241000233622 Phytophthora infestans Species 0.000 description 1
241000233624 Phytophthora megasperma Species 0.000 description 1
241000626605 Phytophthora phaseoli Species 0.000 description 1
241000031556 Phytophthora sp. Species 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
241000758706 Piperaceae Species 0.000 description 1
241001281802 Pseudoperonospora Species 0.000 description 1
241000813090 Rhizoctonia solani Species 0.000 description 1
241000221696 Sclerotinia sclerotiorum Species 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
240000003768 Solanum lycopersicum Species 0.000 description 1
244000299461 Theobroma cacao Species 0.000 description 1
235000005764 Theobroma cacao ssp. cacao Nutrition 0.000 description 1
235000005767 Theobroma cacao ssp. sphaerocarpum Nutrition 0.000 description 1
241000221576 Uromyces Species 0.000 description 1
241000221577 Uromyces appendiculatus Species 0.000 description 1
241000082085 Verticillium <Phyllachorales> Species 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
239000008272 agar Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
239000011717 all-trans-retinol Substances 0.000 description 1
235000019169 all-trans-retinol Nutrition 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 description 1
MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 description 1
235000001046 cacaotero Nutrition 0.000 description 1
JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 description 1
229940117949 captan Drugs 0.000 description 1
TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
235000020971 citrus fruits Nutrition 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
229940125782 compound 2 Drugs 0.000 description 1
229940126214 compound 3 Drugs 0.000 description 1
229940125898 compound 5 Drugs 0.000 description 1
238000009109 curative therapy Methods 0.000 description 1
230000034994 death Effects 0.000 description 1
RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 description 1
238000007865 diluting Methods 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000012990 dithiocarbamate Substances 0.000 description 1
150000004659 dithiocarbamates Chemical class 0.000 description 1
239000004492 dustable powder Substances 0.000 description 1
238000010410 dusting Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
238000011534 incubation Methods 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
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 1
150000002576 ketones Chemical class 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000008268 mayonnaise Substances 0.000 description 1
235000010746 mayonnaise Nutrition 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
AGZFDMRWOVHNRR-UHFFFAOYSA-N methyl n-(1h-benzimidazol-2-yl)-n-(butylcarbamoyl)carbamate Chemical compound C1=CC=C2NC(N(C(=O)OC)C(=O)NCCCC)=NC2=C1 AGZFDMRWOVHNRR-UHFFFAOYSA-N 0.000 description 1
230000017074 necrotic cell death Effects 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000012875 nonionic emulsifier Substances 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
239000007764 o/w emulsion Substances 0.000 description 1
150000007530 organic bases Chemical group 0.000 description 1
230000035515 penetration Effects 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 1
231100000208 phytotoxic Toxicity 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
235000021012 strawberries Nutrition 0.000 description 1
STEHYQULPDKKHF-UHFFFAOYSA-N sulfane;toluene Chemical compound S.CC1=CC=CC=C1 STEHYQULPDKKHF-UHFFFAOYSA-N 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
239000013008 thixotropic agent Substances 0.000 description 1
CENHPXAQKISCGD-UHFFFAOYSA-N trioxathietane 4,4-dioxide Chemical compound O=S1(=O)OOO1 CENHPXAQKISCGD-UHFFFAOYSA-N 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
230000001018 virulence Effects 0.000 description 1
239000007762 w/o emulsion Substances 0.000 description 1
239000001993 wax 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus as a ring member
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
- C07F9/657109—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms esters of oxyacids of phosphorus in which one or more exocyclic oxygen atoms have been replaced by (a) sulfur atom(s)
- C07F9/657118—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms esters of oxyacids of phosphorus in which one or more exocyclic oxygen atoms have been replaced by (a) sulfur atom(s) non-condensed with carbocyclic rings or heterocyclic rings or ring systems
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S424/00—Drug, bio-affecting and body treating compositions
- Y10S424/08—Systemic pesticides

Landscapes

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

CS76642A 1975-02-05 1976-02-02 Fungicide CS196301B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR7504394A FR2299810A1 (fr)	1975-02-05	1975-02-05	Compositions fongicides a base de thiophosphites cycliques

Publications (1)

Publication Number	Publication Date
CS196301B2 true CS196301B2 (en)	1980-03-31

Family

ID=9151127

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS76642A CS196301B2 (en)	1975-02-05	1976-02-02	Fungicide

Country Status (26)

Country	Link
US (1)	US4115559A (fr)
JP (1)	JPS6143321B2 (fr)
AR (1)	AR226670A1 (fr)
AU (1)	AU507473B2 (fr)
BE (1)	BE838297A (fr)
BG (1)	BG28030A3 (fr)
BR (1)	BR7600730A (fr)
CA (1)	CA1055394A (fr)
CH (1)	CH602013A5 (fr)
CS (1)	CS196301B2 (fr)
DD (1)	DD122919A5 (fr)
DE (1)	DE2602804C2 (fr)
ES (1)	ES444932A1 (fr)
FR (1)	FR2299810A1 (fr)
GB (1)	GB1531815A (fr)
GR (1)	GR58540B (fr)
HU (1)	HU175519B (fr)
IL (1)	IL48925A (fr)
IT (1)	IT1060480B (fr)
NL (1)	NL183004C (fr)
OA (1)	OA05236A (fr)
PH (1)	PH13900A (fr)
PL (1)	PL96496B1 (fr)
PT (1)	PT64775B (fr)
SU (1)	SU667107A3 (fr)
ZA (1)	ZA76635B (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4341722A (en) *	1979-07-06	1982-07-27	Ciba-Geigy Corporation	2-Thiono-(2H) [1,3,2] dioxaphosphorinanes (phospholanes)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE548853A (fr)	1955-06-22
DE1926565C3 (de) *	1969-05-23	1974-01-24	Bayer Ag, 5090 Leverkusen	Insektizide Mittel
IL43912A (en) *	1973-01-12	1976-10-31	Pepro	Fungicidal compositions containing phosphites

1975
- 1975-02-05 FR FR7504394A patent/FR2299810A1/fr active Granted
1976
- 1976-01-26 DE DE2602804A patent/DE2602804C2/de not_active Expired
- 1976-01-28 IL IL48925A patent/IL48925A/xx unknown
- 1976-01-30 US US05/654,052 patent/US4115559A/en not_active Expired - Lifetime
- 1976-01-30 NL NLAANVRAGE7600969,A patent/NL183004C/xx not_active IP Right Cessation
- 1976-02-02 CS CS76642A patent/CS196301B2/cs unknown
- 1976-02-02 PH PH18038A patent/PH13900A/en unknown
- 1976-02-03 BG BG032278A patent/BG28030A3/xx unknown
- 1976-02-03 DD DD191068A patent/DD122919A5/xx unknown
- 1976-02-04 GB GB4353/76A patent/GB1531815A/en not_active Expired
- 1976-02-04 JP JP51011817A patent/JPS6143321B2/ja not_active Expired
- 1976-02-04 PL PL1976187019A patent/PL96496B1/pl unknown
- 1976-02-04 CA CA245,027A patent/CA1055394A/fr not_active Expired
- 1976-02-04 PT PT64775A patent/PT64775B/fr unknown
- 1976-02-04 ZA ZA635A patent/ZA76635B/xx unknown
- 1976-02-05 IT IT47964/76A patent/IT1060480B/it active
- 1976-02-05 CH CH142576A patent/CH602013A5/xx not_active IP Right Cessation
- 1976-02-05 ES ES444932A patent/ES444932A1/es not_active Expired
- 1976-02-05 SU SU762319211A patent/SU667107A3/ru active
- 1976-02-05 AR AR262161A patent/AR226670A1/es active
- 1976-02-05 OA OA55730A patent/OA05236A/fr unknown
- 1976-02-05 GR GR49961A patent/GR58540B/el unknown
- 1976-02-05 BE BE164116A patent/BE838297A/fr not_active IP Right Cessation
- 1976-02-05 HU HU76PI508A patent/HU175519B/hu unknown
- 1976-02-05 BR BR7600730A patent/BR7600730A/pt unknown
- 1976-02-05 AU AU10839/76A patent/AU507473B2/en not_active Expired

Also Published As

Publication number	Publication date
IL48925A0 (en)	1976-03-31
IL48925A (en)	1978-06-15
PH13900A (en)	1980-10-27
GB1531815A (en)	1978-11-08
IT1060480B (it)	1982-08-20
DD122919A5 (de)	1976-11-12
PT64775B (fr)	1978-02-03
CH602013A5 (fr)	1978-07-14
DE2602804C2 (de)	1986-09-18
CA1055394A (fr)	1979-05-29
DE2602804A1 (de)	1976-08-19
BR7600730A (pt)	1976-08-31
PT64775A (fr)	1976-03-01
PL96496B1 (pl)	1977-12-31
FR2299810B1 (fr)	1977-07-22
ES444932A1 (es)	1977-10-01
NL7600969A (nl)	1976-08-09
ZA76635B (en)	1977-01-26
NL183004B (nl)	1988-02-01
AU1083976A (en)	1977-08-11
BG28030A3 (en)	1980-02-25
OA05236A (fr)	1981-02-28
NL183004C (nl)	1988-07-01
US4115559A (en)	1978-09-19
AU507473B2 (en)	1980-02-14
SU667107A3 (ru)	1979-06-05
JPS51104034A (fr)	1976-09-14
FR2299810A1 (fr)	1976-09-03
AR226670A1 (es)	1982-08-13
HU175519B (hu)	1980-08-28
GR58540B (en)	1977-10-31
BE838297A (fr)	1976-08-05
JPS6143321B2 (fr)	1986-09-26

Publication	Publication Date	Title
HU184319B (en)	1984-08-28	Fungicide compositions salts of phosphonoic acid-monoesters and process for producing the active agents
DK164157B (da)	1992-05-18	Trialkyl- eller arylsulf(ox)oniumphosphinat-derivater med fungicid aktivitet, fremgangsmaade til fremstilling deraf samt fungicid- og/eller baktericidpraeparater indeholdende de aktive forbindelser og en fremgangsmaade til sygdomsbehandling af plantevaekster
US4076807A (en)	1978-02-28	Phosphite-based fungicide compositions
CA1118785A (fr)	1982-02-23	Derives du type phosphites d'isothiouronium
US7511029B2 (en)	2009-03-31	Pesticidal diazene oxide carboxylates
CS196301B2 (en)	1980-03-31	Fungicide
EP0219192A2 (fr)	1987-04-22	Fongicides
CH631721A5 (de)	1982-08-31	Pflanzenschutzmittel.
US4297367A (en)	1981-10-27	2-Phenyl-4-pyrone derivatives, their preparation and their use as fungicides
US4046883A (en)	1977-09-06	Fungicidal compositions based on polyimides of phosphorus and method of treating plants therewith
US4115582A (en)	1978-09-19	N-1,1,2,2-tetrachloro-2-fluoroethylthio benzanilide and its use as fungicide and acaricide
US3767734A (en)	1973-10-23	Phosphorylated thiourea compositions
US4041109A (en)	1977-08-09	Diphosphorous
CS253744B2 (en)	1987-12-17	Fungicide and plants growth regulator
US3487156A (en)	1969-12-30	Combating insects,their eggs,or acarids on plants
US3005841A (en)	1961-10-24	Bromine-containing organo phosphate
US7399757B1 (en)	2008-07-15	Pesticidal diazene oxide carboxylates
WO1995011899A1 (fr)	1995-05-04	Derives de pyrimidine
US3927219A (en)	1975-12-16	Method of controlling pests with thioureido carbamates compounds
DD149455A5 (de)	1981-07-15	Fungizide zusammensetzung
US3249496A (en)	1966-05-03	Soil fungicide
KR800000222B1 (ko)	1980-03-22	1-페닐-1, 3, 5, 7,-테트라아자-4-설파-헵트-1-엔-6-온 유도체의 제조방법
US2961372A (en)	1960-11-22	Pesticide
US3856502A (en)	1974-12-24	Method for stimulation of plant growth
JPS5912085B2 (ja)	1984-03-21	植物菌類性病害抑制方法