DE1908680A1 - N-Trifluormehtylmercapto-methylmercaptophthalimide,Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide - Google Patents

N-Trifluormehtylmercapto-methylmercaptophthalimide,Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide

Info

Publication number: DE1908680A1
Authority: DE; Germany
Prior art keywords: active ingredient; methylmercaptophthalimide; preparation; fungi; plants
Prior art date: 1969-02-21
Legal status (The legal status 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 status listed.): Pending

Application number

DE19691908680

Other languages

German (de)

English (en)

Inventor

Dr Ferdinand Grewe

Dr Dr Alois Haas

Dr Walter Klug

Dr Engelbert Kuehle

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Bayer AG

Original Assignee

Bayer AG

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

1969-02-21

Filing date

1969-02-21

Publication date

1970-09-10

1969-02-21 Application filed by Bayer AG filed Critical Bayer AG

1969-02-21 Priority to DE19691908680 priority Critical patent/DE1908680A1/de

1970-02-02 Priority to IL33822A priority patent/IL33822A0/xx

1970-02-18 Priority to NL7002283A priority patent/NL7002283A/xx

1970-02-20 Priority to FR7006243A priority patent/FR2032948A5/fr

1970-02-20 Priority to BR216894/70A priority patent/BR7016894D0/pt

1970-02-20 Priority to BE746300D priority patent/BE746300A/fr

1970-09-10 Publication of DE1908680A1 publication Critical patent/DE1908680A1/de

Status Pending legal-status Critical Current

Links

-1 N-Trifluormethylmercapto-methylmercaptophthalimide Chemical compound 0.000 title claims description 14
238000000034 method Methods 0.000 title claims description 10
239000000417 fungicide Substances 0.000 title claims description 6
238000002360 preparation method Methods 0.000 title claims description 4
241000233866 Fungi Species 0.000 claims description 14
XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 4
239000011230 binding agent Substances 0.000 claims description 4
239000004606 Fillers/Extenders Substances 0.000 claims description 3
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
239000011737 fluorine Substances 0.000 claims description 2
229910052731 fluorine Inorganic materials 0.000 claims description 2
FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
235000001674 Agaricus brunnescens Nutrition 0.000 claims 1
239000004480 active ingredient Substances 0.000 description 28
241000196324 Embryophyta Species 0.000 description 15
239000002904 solvent Substances 0.000 description 11
241000220225 Malus Species 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
206010061217 Infestation Diseases 0.000 description 9
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
150000001875 compounds Chemical class 0.000 description 9
239000000203 mixture Substances 0.000 description 9
239000007788 liquid Substances 0.000 description 8
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
239000003995 emulsifying agent Substances 0.000 description 6
239000007921 spray Substances 0.000 description 6
239000000460 chlorine Substances 0.000 description 5
230000000855 fungicidal effect Effects 0.000 description 5
206010039509 Scab Diseases 0.000 description 4
238000009472 formulation Methods 0.000 description 4
238000011081 inoculation Methods 0.000 description 4
230000001681 protective effect Effects 0.000 description 4
239000000725 suspension Substances 0.000 description 4
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
241000489964 Fusicladium Species 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
241000896242 Podosphaera Species 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
238000005507 spraying Methods 0.000 description 3
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
241000221785 Erysiphales Species 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
230000000895 acaricidal effect Effects 0.000 description 2
239000013543 active substance Substances 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
238000010410 dusting Methods 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
230000002464 fungitoxic effect Effects 0.000 description 2
239000008187 granular material Substances 0.000 description 2
208000015181 infectious disease Diseases 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
239000011707 mineral Substances 0.000 description 2
239000006072 paste Substances 0.000 description 2
239000000843 powder Substances 0.000 description 2
239000000243 solution Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
241000235349 Ascomycota Species 0.000 description 1
241000221198 Basidiomycota Species 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
241001480059 Erysiphaceae Species 0.000 description 1
241000221787 Erysiphe Species 0.000 description 1
241000510928 Erysiphe necator Species 0.000 description 1
241000896218 Golovinomyces orontii Species 0.000 description 1
241000238631 Hexapoda Species 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
208000031888 Mycoses Diseases 0.000 description 1
241000896238 Oidium Species 0.000 description 1
241001337928 Podosphaera leucotricha Species 0.000 description 1
241000579741 Sphaerotheca <fungi> Species 0.000 description 1
241001617088 Thanatephorus sasakii Species 0.000 description 1
241000510929 Uncinula Species 0.000 description 1
241000228452 Venturia inaequalis Species 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910001854 alkali hydroxide Inorganic materials 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
238000001816 cooling Methods 0.000 description 1
244000038559 crop plants Species 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
231100000162 fungitoxic Toxicity 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
230000002045 lasting effect Effects 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
230000002175 menstrual effect Effects 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
230000003071 parasitic effect Effects 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
FZUJWWOKDIGOKH-UHFFFAOYSA-N sulfuric acid hydrochloride Chemical compound Cl.OS(O)(=O)=O FZUJWWOKDIGOKH-UHFFFAOYSA-N 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
239000002699 waste material Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Indole Compounds (AREA)

DE19691908680 1969-02-21 1969-02-21 N-Trifluormehtylmercapto-methylmercaptophthalimide,Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide Pending DE1908680A1 (de)

Priority Applications (6)

Application Number	Priority Date	Filing Date	Title
DE19691908680 DE1908680A1 (de)	1969-02-21	1969-02-21	N-Trifluormehtylmercapto-methylmercaptophthalimide,Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
IL33822A IL33822A0 (en)	1969-02-21	1970-02-02	N-substituted phthalimides,their preparation and their use as fungicides
NL7002283A NL7002283A (fr)	1969-02-21	1970-02-18
FR7006243A FR2032948A5 (en)	1969-02-21	1970-02-20	Fungicidal phthalimide derivs
BR216894/70A BR7016894D0 (pt)	1969-02-21	1970-02-20	Processo para a preparacao de novas n-trifluor-metilmercapto-metilmercaptoftalimidas bem como composicoes fungicidas a base das mesmas
BE746300D BE746300A (fr)	1969-02-21	1970-02-20	Nouveaux n-trifluormethylmercapto-methylmercapto-phtalimides, leur procede de preparation et leur application a la lutte contre deschampignon

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19691908680 DE1908680A1 (de)	1969-02-21	1969-02-21	N-Trifluormehtylmercapto-methylmercaptophthalimide,Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide

Publications (1)

Publication Number	Publication Date
DE1908680A1 true DE1908680A1 (de)	1970-09-10

Family

ID=5725892

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE19691908680 Pending DE1908680A1 (de)	1969-02-21	1969-02-21	N-Trifluormehtylmercapto-methylmercaptophthalimide,Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide

Country Status (6)

Country	Link
BE (1)	BE746300A (fr)
BR (1)	BR7016894D0 (fr)
DE (1)	DE1908680A1 (fr)
FR (1)	FR2032948A5 (fr)
IL (1)	IL33822A0 (fr)
NL (1)	NL7002283A (fr)

1969
- 1969-02-21 DE DE19691908680 patent/DE1908680A1/de active Pending
1970
- 1970-02-02 IL IL33822A patent/IL33822A0/xx unknown
- 1970-02-18 NL NL7002283A patent/NL7002283A/xx unknown
- 1970-02-20 BE BE746300D patent/BE746300A/fr unknown
- 1970-02-20 BR BR216894/70A patent/BR7016894D0/pt unknown
- 1970-02-20 FR FR7006243A patent/FR2032948A5/fr not_active Expired

Also Published As

Publication number	Publication date
NL7002283A (fr)	1970-08-25
BR7016894D0 (pt)	1973-03-08
BE746300A (fr)	1970-08-20
IL33822A0 (en)	1970-04-20
FR2032948A5 (en)	1970-11-27

Publication	Publication Date	Title
DE2206010A1 (de)	1973-08-16	1-aminosulfonyl-2-amino-benzimidazole, verfahren zu ihrer herstellung und ihre fungizide verwendung
DE2431073A1 (de)	1976-01-15	Fungizides mittel
DE2648074A1 (de)	1978-04-27	N-chloracetyl-n-phenyl-alaninester, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide
DE2201062A1 (de)	1973-07-26	N-alkoxycarbonyl- bzw. n-alkylthiocarbonyl-2-(2'-thienyl)-benzimidazole, ein verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE1908680A1 (de)	1970-09-10	N-Trifluormehtylmercapto-methylmercaptophthalimide,Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
DE2025413A1 (de)	1971-12-02	Ureidophenylisothioharnstoffe, Verfahren zu ihrer Herstellung und ihre fungizide Verwendung
DD209717A5 (de)	1984-05-23	Schaedlingsbekaempfungsmittel
EP0009569A1 (fr)	1980-04-16	Dérivés oxalyliques d'acides N-phénylaminocarboxyliques (et leurs esters), procédés pour leur préparation et leur utilisation comme fongicides
DE2126149A1 (en)	1972-12-07	Halo-salicylanilide derivs - with acaricidal and fungicidal activity
EP0003520B1 (fr)	1981-07-15	Dérivés spiro de 3-(3,5-dihalogénophényl)-oxazolidin-2,4-diones, leurs procédés de préparation et leur application comme fongicides
DE2025412A1 (de)	1971-12-02	Amidophenylisothiohamstoffe, Verfahren zu ihrer Herstellung und ihre fungizide Verwendung
DE1950100B2 (de)	1976-12-02	Verwendung von 2-chloraethan-(thiono)- phosphonsaeureamido-verbindungen zur beeinflussung des pflanzenwachstums
DE2740848A1 (de)	1979-03-29	Substituierte n-phenyl-bernsteinsaeureimide, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide
DE1670705A1 (de)	1970-11-12	Verfahren zur Herstellung von N-substituierten Phthalimiden
DE1668085A1 (de)	1971-04-15	O-Halogenphenyl-carbamate
DE2242785A1 (de)	1974-03-14	1-alkylsulfonyl-2-trifluormethylbenzimidazole, verfahren zu ihrer herstellung sowie ihre verwendung als ektoparasitenmittel
DE1543604C3 (fr)	1974-11-21
DE2410184A1 (de)	1975-10-02	Chinonoxim-acylhydrazon-derivate, verfahren zu ihrer herstellung, sowie ihre verwendung als fungizide
DE2064596C3 (de)	1975-10-02	3- eckige Klammer auf N-(Fluordichlormethylthio) -N- (trifluormethyl) -amino eckige Klammer zu -benzoesäureisopropytamid, Verfahren zu dessen Herste lung und desse n Verwendung
DE2022494A1 (de)	1971-11-18	Fungizide Mittel
EP0014887B1 (fr)	1981-10-14	Dérivés spiro de 3-(3,5-dihalogénophényl)-oxazolidine-2-thion-4-ones, procédés pour leur préparation et leur utilisation comme fongicides
EP0012261A1 (fr)	1980-06-25	Dérivés spiro substitués de 3-(3,5-dichlorophényl)-2,4-oxazolidine diones, procédés pour leur préparation et leur utilisation comme fongicides
DE2141061A1 (de)	1973-02-22	Butensulfonanilid-n-sulfenyl-verbindungen, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE1903169C (de)	1973-05-24	Fungizides Mittel
EP0161480B1 (fr)	1987-06-03	N-iodepropargyl-chlorométhanesulfonamide