CH561182A5 - Dichloromaleimide derivs - with biocidal activity - Google Patents

Dichloromaleimide derivs - with biocidal activity

Info

Publication number: CH561182A5
Authority: CH; Switzerland
Prior art keywords: sep; formula; hydrogen; compounds; dichloromaleimide
Prior art date: 1972-01-12

Application number

CH43872A

Other languages

German (de)

English (en)

Original Assignee

Ciba Geigy Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1972-01-12

Filing date

1972-01-12

Publication date

1975-04-30

1972-01-12 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1972-01-12 Priority to CH43872A priority Critical patent/CH561182A5/de

1972-12-25 Priority to IL41159A priority patent/IL41159A/en

1972-12-29 Priority to IT33998/72A priority patent/IT987595B/it

1973-01-08 Priority to US321624A priority patent/US3894043A/en

1973-01-09 Priority to CS19173A priority patent/CS169834B2/cs

1973-01-09 Priority to DE2300913A priority patent/DE2300913A1/de

1973-01-10 Priority to NL7300364A priority patent/NL7300364A/xx

1973-01-11 Priority to BE793890D priority patent/BE793890A/xx

1973-01-11 Priority to JP48006275A priority patent/JPS4877027A/ja

1973-01-11 Priority to FR7300858A priority patent/FR2167943B1/fr

1973-01-11 Priority to AT22973A priority patent/AT321643B/de

1973-01-11 Priority to HUCI001329 priority patent/HU165671B/hu

1973-01-11 Priority to GB157173A priority patent/GB1394619A/en

1975-04-17 Priority to US05/568,946 priority patent/US3980798A/en

1975-04-30 Publication of CH561182A5 publication Critical patent/CH561182A5/de

Links

KVBAKSQRUXXHCK-UHFFFAOYSA-N 3,4-Dichloro-5-hydroxy-2H-pyrrol-2-one Chemical compound ClC1=C(Cl)C(=O)NC1=O KVBAKSQRUXXHCK-UHFFFAOYSA-N 0.000 title claims description 3
230000003115 biocidal effect Effects 0.000 title description 3
241000233866 Fungi Species 0.000 claims abstract description 11
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 10
229910052736 halogen Inorganic materials 0.000 claims abstract description 5
150000002367 halogens Chemical class 0.000 claims abstract description 5
239000002253 acid Substances 0.000 claims abstract description 3
230000003032 phytopathogenic effect Effects 0.000 claims abstract description 3
150000001875 compounds Chemical class 0.000 claims description 21
-1 ethylidene, trimethylene Chemical group 0.000 claims description 13
239000001257 hydrogen Substances 0.000 claims description 9
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 5
150000002431 hydrogen Chemical class 0.000 claims description 4
238000002360 preparation method Methods 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
238000000034 method Methods 0.000 claims description 3
229910052760 oxygen Inorganic materials 0.000 claims description 3
239000001301 oxygen Substances 0.000 claims description 3
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 2
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
229910052794 bromium Inorganic materials 0.000 abstract description 4
229910052801 chlorine Inorganic materials 0.000 abstract description 4
AGULWIQIYWWFBJ-UHFFFAOYSA-N 3,4-dichlorofuran-2,5-dione Chemical compound ClC1=C(Cl)C(=O)OC1=O AGULWIQIYWWFBJ-UHFFFAOYSA-N 0.000 abstract description 3
229910052717 sulfur Inorganic materials 0.000 abstract description 3
230000000694 effects Effects 0.000 abstract description 2
150000001412 amines Chemical class 0.000 abstract 1
239000000417 fungicide Substances 0.000 abstract 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 12
241000196324 Embryophyta Species 0.000 description 11
239000013543 active substance Substances 0.000 description 11
239000000126 substance Substances 0.000 description 8
239000000725 suspension Substances 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
239000004480 active ingredient Substances 0.000 description 5
239000004563 wettable powder Substances 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
241001465754 Metazoa Species 0.000 description 4
239000000969 carrier Substances 0.000 description 4
239000008187 granular material Substances 0.000 description 4
208000015181 infectious disease Diseases 0.000 description 4
239000000203 mixture Substances 0.000 description 4
238000005507 spraying Methods 0.000 description 4
241000894006 Bacteria Species 0.000 description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
241000221561 Ustilaginales Species 0.000 description 3
229960000583 acetic acid Drugs 0.000 description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
238000011156 evaluation Methods 0.000 description 3
239000012362 glacial acetic acid Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 3
241000223600 Alternaria Species 0.000 description 2
240000007087 Apium graveolens Species 0.000 description 2
241001465180 Botrytis Species 0.000 description 2
241000123650 Botrytis cinerea Species 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
240000007594 Oryza sativa Species 0.000 description 2
244000046052 Phaseolus vulgaris Species 0.000 description 2
241000233626 Plasmopara Species 0.000 description 2
241000540505 Puccinia dispersa f. sp. tritici Species 0.000 description 2
241001533598 Septoria Species 0.000 description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
241000228395 Taphrinales Species 0.000 description 2
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235000013399 edible fruits Nutrition 0.000 description 2
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125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
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238000003756 stirring Methods 0.000 description 2
239000011593 sulfur Chemical group 0.000 description 2
208000024891 symptom Diseases 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
241000323752 Alternaria longipes Species 0.000 description 1
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239000005995 Aluminium silicate Substances 0.000 description 1
241000415078 Anemone hepatica Species 0.000 description 1
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235000015849 Apium graveolens Dulce Group Nutrition 0.000 description 1
235000010591 Appio Nutrition 0.000 description 1
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VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
241001126310 Fasciolidae Species 0.000 description 1
241000282326 Felis catus Species 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
241000223218 Fusarium Species 0.000 description 1
241000611205 Fusarium oxysporum f. sp. lycopersici Species 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
241000896246 Golovinomyces cichoracearum Species 0.000 description 1
241001499731 Gyrosigma fasciola Species 0.000 description 1
241000221661 Helotiales Species 0.000 description 1
241001464384 Hymenolepis nana Species 0.000 description 1
241000208822 Lactuca Species 0.000 description 1
241000243789 Metastrongyloidea Species 0.000 description 1
241000223607 Microascales Species 0.000 description 1
241000186359 Mycobacterium Species 0.000 description 1
241000193034 Myriangiales Species 0.000 description 1
241000244206 Nematoda Species 0.000 description 1
241001219479 Olpidium Species 0.000 description 1
241000233654 Oomycetes Species 0.000 description 1
241000190509 Ophiobolus Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
241001494479 Pecora Species 0.000 description 1
241000221700 Pezizales Species 0.000 description 1
241001674143 Phacidiales Species 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
BHHGXPLMPWCGHP-UHFFFAOYSA-N Phenethylamine Chemical compound NCCC1=CC=CC=C1 BHHGXPLMPWCGHP-UHFFFAOYSA-N 0.000 description 1
241000975369 Phoma betae Species 0.000 description 1
241001294742 Podosphaera macularis Species 0.000 description 1
241000222383 Polyporales Species 0.000 description 1
241000221300 Puccinia Species 0.000 description 1
244000309617 Puccinia cacabata Species 0.000 description 1
241001123561 Puccinia coronata Species 0.000 description 1
241000221301 Puccinia graminis Species 0.000 description 1
241000221535 Pucciniales Species 0.000 description 1
206010037888 Rash pustular Diseases 0.000 description 1
241000813090 Rhizoctonia solani Species 0.000 description 1
241000235343 Saccharomycetales Species 0.000 description 1
241000242679 Schistosoma bovis Species 0.000 description 1
241001442514 Schistosomatidae Species 0.000 description 1
241001558929 Sclerotium <basidiomycota> Species 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
241001051088 Sphaerotheca humuli Species 0.000 description 1
241000186652 Sporosarcina ureae Species 0.000 description 1
241000191940 Staphylococcus Species 0.000 description 1
241001126266 Strongyloidea Species 0.000 description 1
241000282887 Suidae Species 0.000 description 1
241000244161 Taeniidae Species 0.000 description 1
241001494489 Thielavia Species 0.000 description 1
241000865903 Thielaviopsis Species 0.000 description 1
241000722133 Tilletia Species 0.000 description 1
241000869417 Trematodes Species 0.000 description 1
241000221365 Tremellales Species 0.000 description 1
241000243793 Trichostrongyloidea Species 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
241001091387 Uromyces beticola Species 0.000 description 1
241000221566 Ustilago Species 0.000 description 1
241000514371 Ustilago avenae Species 0.000 description 1
241000509513 Ustilago hordei Species 0.000 description 1
241000233791 Ustilago tritici Species 0.000 description 1
241000082085 Verticillium <Phyllachorales> Species 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
HUMHYXGDUOGHTG-HEZXSMHISA-N alpha-D-GalpNAc-(1->3)-[alpha-L-Fucp-(1->2)]-D-Galp Chemical compound O[C@H]1[C@H](O)[C@H](O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](O[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](O)[C@@H](CO)OC1O HUMHYXGDUOGHTG-HEZXSMHISA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
230000000507 anthelmentic effect Effects 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
235000012216 bentonite Nutrition 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
229910000389 calcium phosphate Inorganic materials 0.000 description 1
235000011010 calcium phosphates Nutrition 0.000 description 1
239000002775 capsule Substances 0.000 description 1
150000001720 carbohydrates Chemical class 0.000 description 1
235000014633 carbohydrates Nutrition 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
235000012343 cottonseed oil Nutrition 0.000 description 1
238000005520 cutting process Methods 0.000 description 1
230000000249 desinfective effect Effects 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
235000021186 dishes Nutrition 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
238000000227 grinding Methods 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
238000011534 incubation Methods 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 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
235000009973 maize Nutrition 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
239000006072 paste Substances 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
244000144977 poultry Species 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
208000029561 pustule Diseases 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
230000009291 secondary effect Effects 0.000 description 1
UQDJGEHQDNVPGU-UHFFFAOYSA-N serine phosphoethanolamine Chemical compound [NH3+]CCOP([O-])(=O)OCC([NH3+])C([O-])=O UQDJGEHQDNVPGU-UHFFFAOYSA-N 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
235000002639 sodium chloride Nutrition 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
239000003826 tablet Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
235000012222 talc Nutrition 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/44—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members
- C07D207/444—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5
- C07D207/456—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5 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 other ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2696—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds characterised by the process or apparatus used

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

CH43872A 1972-01-12 1972-01-12 Dichloromaleimide derivs - with biocidal activity CH561182A5 (en)

Priority Applications (14)

Application Number	Priority Date	Filing Date	Title
CH43872A CH561182A5 (en)	1972-01-12	1972-01-12	Dichloromaleimide derivs - with biocidal activity
IL41159A IL41159A (en)	1972-01-12	1972-12-25	Dichloromaleic acid imides,their preparation and their use in the control of plant pathogenic fungi
IT33998/72A IT987595B (it)	1972-01-12	1972-12-29	Dioloro malein immidi loro preparazione e loro impiego per combattere organismi nocivi
US321624A US3894043A (en)	1972-01-12	1973-01-08	New imides, their manufacture and their use as microbiocides
CS19173A CS169834B2 (cs)	1972-01-12	1973-01-09
DE2300913A DE2300913A1 (de)	1972-01-12	1973-01-09	Neue imide
NL7300364A NL7300364A (cs)	1972-01-12	1973-01-10
BE793890D BE793890A (fr)	1972-01-12	1973-01-11	Imides substitues a l'azote et produits fongicides a usages phytopharmaceutiques
JP48006275A JPS4877027A (cs)	1972-01-12	1973-01-11
FR7300858A FR2167943B1 (cs)	1972-01-12	1973-01-11
AT22973A AT321643B (de)	1972-01-12	1973-01-11	Mittel zur Bekämpfung phytopathogener Pilze
HUCI001329 HU165671B (cs)	1972-01-12	1973-01-11
GB157173A GB1394619A (en)	1972-01-12	1973-01-11	Imides
US05/568,946 US3980798A (en)	1972-01-12	1975-04-17	Dichloromaleic imides for fungicidal composition and method

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH43872A CH561182A5 (en)	1972-01-12	1972-01-12	Dichloromaleimide derivs - with biocidal activity

Publications (1)

Publication Number	Publication Date
CH561182A5 true CH561182A5 (en)	1975-04-30

Family

ID=4187028

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH43872A CH561182A5 (en)	1972-01-12	1972-01-12	Dichloromaleimide derivs - with biocidal activity

Country Status (4)

Country	Link
AT (1)	AT321643B (cs)
CH (1)	CH561182A5 (cs)
CS (1)	CS169834B2 (cs)
HU (1)	HU165671B (cs)

1972
- 1972-01-12 CH CH43872A patent/CH561182A5/de not_active IP Right Cessation
1973
- 1973-01-09 CS CS19173A patent/CS169834B2/cs unknown
- 1973-01-11 AT AT22973A patent/AT321643B/de not_active IP Right Cessation
- 1973-01-11 HU HUCI001329 patent/HU165671B/hu unknown

Also Published As

Publication number	Publication date
CS169834B2 (cs)	1976-07-29
HU165671B (cs)	1974-10-28
AT321643B (de)	1975-04-10

Legal Events

Date	Code	Title	Description
1978-09-15	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
EP0450355B1 (de)	1995-08-09	Verbindungen zur Bekämpfung von Pflanzenkrankheiten
DE3788912T2 (de)	1994-05-11	Pyrimidin-Derivate, Verfahren zu deren Herstellung und diese als wirksamen Bestandteil enthaltende Pflanzenkrankheiten-Schutzmittel.
EP0120321A1 (de)	1984-10-03	Acrylsäureamide, ihre Herstellung und Verwendung
EP0007482A1 (de)	1980-02-06	2-Chlor-6-nitroaniline, Verfahren zu ihrer Herstellung, ihre Verwendung, herbizide Mittel
DE3109035A1 (de)	1982-01-07	N-substituierte-(delta)(pfeil hoch)1(pfeil hoch)tetrahydrophthalimidderivate, diese enthaltende herbizide zusammensetzung und verfahren zu deren verwendung
DD155713A5 (de)	1982-06-30	Fungizide zusammensetzung
DD144498A5 (de)	1980-10-22	Verfahren zur verringerung von herbizidschaeden
DD149013A5 (de)	1981-06-24	Herbizides und pflanzenregulierendes mittel
DE3883695T2 (de)	1994-02-17	Amid-Derivate, Verfahren zu deren Herstellung sowie diese enthaltende Fungizide in der Agrikultur und im Gartenbau.
DE2212558A1 (de)	1972-10-05	Herbizide Mittel und ein Verfahren zur Herstellung neuer herbizider Wirkstoffe
DE2843291A1 (de)	1979-04-12	Phenylisothiocyanate und deren salze, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE2223644A1 (de)	1972-11-30	Mittel zur Beeinflussung des Pflanzenwachstums
DE2525855C3 (de)	1978-06-22	Substituierte Benzoesäureanilide sowie ein diese Verbindungen enthaltendes Mittel
DE2643403C2 (de)	1987-01-22	Thiocarbonsäurederivate, Verfahren zu deren Herstellung und diese enthaltende Mittel
CH637386A5 (de)	1983-07-29	Benzoxazol- und benzothiazolderivate.
DE2212827A1 (de)	1972-09-28	Pflanzenschutzmittel
DE69823191T2 (de)	2004-08-19	1,2,3-thiadiazol-derivate, mittel zur kontrolle von pflanzenkrankheiten und methode zu seiner anwendung
EP0092112B1 (de)	1985-03-06	Substituierte Phenoxypropionate
EP0003430B1 (en)	1982-01-06	Novel 2,6-dinitrobenzenamines, their preparation, composition containing them and their use as fungicides
US3707366A (en)	1972-12-26	Pre-emergent chemical method of combating unwanted vegetation
DD246022A5 (de)	1987-05-27	Fungizides mittel
EP0011802B1 (de)	1982-09-15	Neue Phenoxy-phenoxypropionsäureamide, Verfahren zu ihrer Herstellung, sie enthaltende herbizide Mittel und ihre Verwendung zur Bekämpfung von Schadpflanzen
DE2812957A1 (de)	1978-10-12	N-disubstituierte anilin-derivate, verfahren zu ihrer herstellung und mikrobizide mittel
DE2643445C2 (de)	1987-01-29	N-Acylierte N-Phenyl-alaninthiomethylester, Verfahren zu deren Herstellung und diese enthaltende Mittel
DE69625702T2 (de)	2003-10-09	N-((fluoroalkoxy)phenoxyalkyl)benzamidverbindungen, ihre zwischenprodukte, verfahren zur ihrer herstellung und landwirtschaftliche und gartenbauliche pestizide