CH618679A5 - - Google Patents

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Info

Publication number: CH618679A5
Authority: CH; Switzerland
Prior art keywords: compound; formula; compounds; wood; chloroform
Prior art date: 1975-11-25

Application number

CH1466476A

Other languages

English (en)

French (fr)

Inventor

Hans Berg Madsen

Per Dausell Klemmensen

Hans Kolind-Andersen

Original Assignee

Cheminova As

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.)

1975-11-25

Filing date

1976-11-22

Publication date

1980-08-15

1975-11-25 Priority claimed from GB48441/75A external-priority patent/GB1499169A/en

1976-11-22 Application filed by Cheminova As filed Critical Cheminova As

1980-08-15 Publication of CH618679A5 publication Critical patent/CH618679A5/fr

Links

150000001875 compounds Chemical class 0.000 claims description 62
239000000203 mixture Substances 0.000 claims description 21
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 20
238000000034 method Methods 0.000 claims description 17
-1 haloethyl thiochloride Chemical compound 0.000 claims description 12
239000002023 wood Substances 0.000 claims description 12
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 9
238000002360 preparation method Methods 0.000 claims description 9
229910052757 nitrogen Inorganic materials 0.000 claims description 6
150000001408 amides Chemical class 0.000 claims description 5
CIFFBTOJCKSRJY-UHFFFAOYSA-N 3α,4,7,7α-tetrahydro-1h-isoindole-1,3(2h)-dione Chemical compound C1C=CCC2C(=O)NC(=O)C21 CIFFBTOJCKSRJY-UHFFFAOYSA-N 0.000 claims description 4
230000000895 acaricidal effect Effects 0.000 claims description 4
238000006243 chemical reaction Methods 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
125000001153 fluoro group Chemical group F* 0.000 claims description 4
125000005843 halogen group Chemical group 0.000 claims description 4
239000000642 acaricide Substances 0.000 claims description 3
229910052731 fluorine Inorganic materials 0.000 claims description 3
239000000417 fungicide Substances 0.000 claims description 3
150000003949 imides Chemical class 0.000 claims description 3
XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims description 3
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
239000011541 reaction mixture Substances 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
125000004969 haloethyl group Chemical group 0.000 claims 1
229910052739 hydrogen Inorganic materials 0.000 claims 1
239000001257 hydrogen Substances 0.000 claims 1
FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 claims 1
239000000460 chlorine Substances 0.000 description 19
241000233866 Fungi Species 0.000 description 11
239000007788 liquid Substances 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
230000000855 fungicidal effect Effects 0.000 description 8
240000005979 Hordeum vulgare Species 0.000 description 7
235000007340 Hordeum vulgare Nutrition 0.000 description 7
240000007594 Oryza sativa Species 0.000 description 6
235000007164 Oryza sativa Nutrition 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
SVIKNKPDPGCMAE-UHFFFAOYSA-N n-phenyl-n-(1,1,2,2-tetrachloro-2-fluoroethyl)sulfanylmethanesulfonamide Chemical compound FC(Cl)(Cl)C(Cl)(Cl)SN(S(=O)(=O)C)C1=CC=CC=C1 SVIKNKPDPGCMAE-UHFFFAOYSA-N 0.000 description 6
235000009566 rice Nutrition 0.000 description 6
238000011282 treatment Methods 0.000 description 6
239000011230 binding agent Substances 0.000 description 5
ZRDUSMYWDRPZRM-UHFFFAOYSA-N 2-sec-butyl-4,6-dinitrophenyl 3-methylbut-2-enoate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)C=C(C)C ZRDUSMYWDRPZRM-UHFFFAOYSA-N 0.000 description 4
241001600093 Coniophora Species 0.000 description 4
244000141359 Malus pumila Species 0.000 description 4
235000011430 Malus pumila Nutrition 0.000 description 4
235000015103 Malus silvestris Nutrition 0.000 description 4
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
241000209140 Triticum Species 0.000 description 4
235000021307 Triticum Nutrition 0.000 description 4
239000013078 crystal Substances 0.000 description 4
230000000694 effects Effects 0.000 description 4
229930195733 hydrocarbon Natural products 0.000 description 4
150000002430 hydrocarbons Chemical class 0.000 description 4
IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 4
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 3
241000238876 Acari Species 0.000 description 3
241000196324 Embryophyta Species 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
240000008042 Zea mays Species 0.000 description 3
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
235000002017 Zea mays subsp mays Nutrition 0.000 description 3
239000004480 active ingredient Substances 0.000 description 3
229920000180 alkyd Polymers 0.000 description 3
235000005822 corn Nutrition 0.000 description 3
YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 3
229920000940 maneb Polymers 0.000 description 3
239000003921 oil Substances 0.000 description 3
235000019198 oils Nutrition 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
229910052938 sodium sulfate Inorganic materials 0.000 description 3
235000011152 sodium sulphate Nutrition 0.000 description 3
ZEVCJZRMCOYJSP-UHFFFAOYSA-N sodium;2-(dithiocarboxyamino)ethylcarbamodithioic acid Chemical compound [Na+].SC(=S)NCCNC(S)=S ZEVCJZRMCOYJSP-UHFFFAOYSA-N 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
238000005406 washing Methods 0.000 description 3
230000004580 weight loss Effects 0.000 description 3
241000228245 Aspergillus niger Species 0.000 description 2
125000006414 CCl Chemical group ClC* 0.000 description 2
239000005745 Captan Substances 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
239000007832 Na2SO4 Substances 0.000 description 2
241000233679 Peronosporaceae Species 0.000 description 2
235000008331 Pinus X rigitaeda Nutrition 0.000 description 2
241000018646 Pinus brutia Species 0.000 description 2
235000011613 Pinus brutia Nutrition 0.000 description 2
241000157667 Urocystis occulta Species 0.000 description 2
238000013019 agitation Methods 0.000 description 2
229940117949 captan Drugs 0.000 description 2
229940125904 compound 1 Drugs 0.000 description 2
238000002425 crystallisation Methods 0.000 description 2
230000008025 crystallization Effects 0.000 description 2
230000003111 delayed effect Effects 0.000 description 2
208000002925 dental caries Diseases 0.000 description 2
238000011534 incubation Methods 0.000 description 2
230000009545 invasion Effects 0.000 description 2
239000000944 linseed oil Substances 0.000 description 2
235000021388 linseed oil Nutrition 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
238000002156 mixing Methods 0.000 description 2
LBTPIFQNEKOAIM-UHFFFAOYSA-N n-phenylmethanesulfonamide Chemical compound CS(=O)(=O)NC1=CC=CC=C1 LBTPIFQNEKOAIM-UHFFFAOYSA-N 0.000 description 2
239000012044 organic layer Substances 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
239000004033 plastic Substances 0.000 description 2
239000002689 soil Substances 0.000 description 2
239000007858 starting material Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
HNZCHWOSESAIJA-UHFFFAOYSA-N (3-chlorophenyl)methanesulfonamide Chemical compound NS(=O)(=O)CC1=CC=CC(Cl)=C1 HNZCHWOSESAIJA-UHFFFAOYSA-N 0.000 description 1
AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 1
GQHOVWQXQXDLSY-UHFFFAOYSA-N 1-chloro-n-phenyl-n-(1,1,2-trichloro-2,2-difluoroethyl)sulfanylmethanesulfonamide Chemical compound FC(F)(Cl)C(Cl)(Cl)SN(S(=O)(=O)CCl)C1=CC=CC=C1 GQHOVWQXQXDLSY-UHFFFAOYSA-N 0.000 description 1
NZUXRGMXFCTGBV-UHFFFAOYSA-N 2-(1,1,2,2-tetrachloroethylsulfanyl)-3a,4,5,7a-tetrahydroisoindole-1,3-dione Chemical compound C1CC=CC2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)C21 NZUXRGMXFCTGBV-UHFFFAOYSA-N 0.000 description 1
NLGZRKQHMNPTGW-UHFFFAOYSA-N 2-(1,1,2-trichloro-2,2-difluoroethyl)sulfanylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)C(F)(Cl)F)C(=O)C2=C1 NLGZRKQHMNPTGW-UHFFFAOYSA-N 0.000 description 1
QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-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
229920001817 Agar Polymers 0.000 description 1
241000094558 Antrodia sinuosa Species 0.000 description 1
241000228212 Aspergillus Species 0.000 description 1
241000193738 Bacillus anthracis Species 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
240000000731 Fagus sylvatica Species 0.000 description 1
235000010099 Fagus sylvatica Nutrition 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
241000228143 Penicillium Species 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
241000228454 Pyrenophora graminea Species 0.000 description 1
206010039509 Scab Diseases 0.000 description 1
241001674251 Serpula lacrymans Species 0.000 description 1
241001454293 Tetranychus urticae Species 0.000 description 1
APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 1
241000228452 Venturia inaequalis Species 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000008272 agar Substances 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
150000003857 carboxamides Chemical class 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
230000001143 conditioned effect Effects 0.000 description 1
238000010276 construction Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000000875 corresponding effect Effects 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000006073 displacement reaction Methods 0.000 description 1
238000004453 electron probe microanalysis Methods 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
235000019441 ethanol Nutrition 0.000 description 1
125000004705 ethylthio group Chemical group C(C)S* 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
239000011521 glass Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
238000007654 immersion Methods 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
239000010410 layer Substances 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
KJPHTXTWFHVJIG-UHFFFAOYSA-N n-ethyl-2-[(6-methoxypyridin-3-yl)-(2-methylphenyl)sulfonylamino]-n-(pyridin-3-ylmethyl)acetamide Chemical compound C=1C=C(OC)N=CC=1N(S(=O)(=O)C=1C(=CC=CC=1)C)CC(=O)N(CC)CC1=CC=CN=C1 KJPHTXTWFHVJIG-UHFFFAOYSA-N 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
239000004006 olive oil Substances 0.000 description 1
235000008390 olive oil Nutrition 0.000 description 1
125000005543 phthalimide group Chemical class 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000005855 radiation Effects 0.000 description 1
238000002791 soaking Methods 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000012265 solid product Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
230000001954 sterilising effect Effects 0.000 description 1
238000003860 storage Methods 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
239000000725 suspension 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/76—Nitrogen atoms to which a second hetero atom is attached
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B27K3/343—Heterocyclic compounds

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pyridine Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Indole Compounds (AREA)

CH1466476A 1975-11-25 1976-11-22 CH618679A5 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB48441/75A GB1499169A (en)	1975-11-25	1975-11-25	Organic fluoro-imides their preparation and use
GB3582076		1976-08-27

Publications (1)

Publication Number	Publication Date
CH618679A5 true CH618679A5 (de)	1980-08-15

Family

ID=26262871

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1466476A CH618679A5 (de)	1975-11-25	1976-11-22

Country Status (13)

Country	Link
US (1)	US4148901A (de)
JP (1)	JPS5265244A (de)
AT (1)	AT355006B (de)
BR (1)	BR7607880A (de)
CA (1)	CA1079735A (de)
CH (1)	CH618679A5 (de)
DD (1)	DD129283A5 (de)
DE (1)	DE2652451A1 (de)
DK (1)	DK527176A (de)
ES (1)	ES453600A1 (de)
FR (2)	FR2333783A1 (de)
NL (1)	NL7613166A (de)
SU (1)	SU701533A3 (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1499169A (en) *	1975-11-25	1978-01-25	Cheminova As	Organic fluoro-imides their preparation and use
US4282241A (en) *	1975-11-25	1981-08-04	A/S Cheminova	Organic fluoro-imides, their preparation and use
US4210759A (en) *	1978-05-24	1980-07-01	Henkel Corporation	Benzene sulfonamido pyridine derivatives

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1193037B (de) *	1959-11-10	1965-05-20	Bayer Ag	Verfahren zur Herstellung von N-(Polyhalogen-alkansulfenyl)-sulfonsaeureamiden
NL121411C (de) *	1960-08-26
NL271019A (de) *	1960-11-03
DK109482C (da) *	1960-11-03	1968-04-29	Bayer Ag	Fungicid og fremgangsmåder til fremstilling af sulfensyrederivater til anvendelse i fungicidet.
FR1365808A (fr) *	1962-08-08	1964-07-03	Bayer Ag	Agents acaricides
US3314969A (en) *	1963-07-30	1967-04-18	Chevron Res	Process for the preparation of n-polyhaloethylthio compounds
DE1238139B (de) *	1964-04-11	1967-04-06	Bayer Ag	Mikrobizide Mittel fuer Anstriche und Kunststoffueberzuege
AT302721B (de) *	1967-10-05	1972-10-25	Stauffer Chemical Co	Mittel zur Bekämpfung von Milben und Pilzen
IL30807A0 (en) *	1967-10-05	1968-12-26	Stauffer Chemical Co	(tetrachloro-fluoro-ethyl-thio)-n-phenyl sulfamides and their use in controlling pests
US3840555A (en) *	1971-03-10	1974-10-08	Stauffer Chemical Co	Miticidal active fluoro phthalimide derivatives
US4092429A (en) *	1976-02-09	1978-05-30	Stauffer Chemical Company	(Tetrachloro-fluoro-ethyl-thio)N-phenyl sulfonamides and their use in controlling pests

1976
- 1976-11-17 US US05/742,592 patent/US4148901A/en not_active Expired - Lifetime
- 1976-11-17 DE DE19762652451 patent/DE2652451A1/de not_active Withdrawn
- 1976-11-19 AT AT862276A patent/AT355006B/de not_active IP Right Cessation
- 1976-11-22 CA CA266,200A patent/CA1079735A/en not_active Expired
- 1976-11-22 CH CH1466476A patent/CH618679A5/fr not_active IP Right Cessation
- 1976-11-23 DK DK527176A patent/DK527176A/da unknown
- 1976-11-24 DD DD7600195939A patent/DD129283A5/de unknown
- 1976-11-24 BR BR7607880A patent/BR7607880A/pt unknown
- 1976-11-24 ES ES453600A patent/ES453600A1/es not_active Expired
- 1976-11-25 SU SU762425174A patent/SU701533A3/ru active
- 1976-11-25 FR FR7635597A patent/FR2333783A1/fr not_active Withdrawn
- 1976-11-25 NL NL7613166A patent/NL7613166A/xx not_active Application Discontinuation
- 1976-11-25 JP JP51141749A patent/JPS5265244A/ja active Pending
1977
- 1977-05-06 FR FR7713945A patent/FR2339599A1/fr active Granted

Also Published As

Publication number	Publication date
DK527176A (da)	1977-05-26
BR7607880A (pt)	1977-10-25
SU701533A3 (ru)	1979-11-30
CA1079735A (en)	1980-06-17
ATA862276A (de)	1979-07-15
ES453600A1 (es)	1977-11-16
FR2339599A1 (fr)	1977-08-26
AT355006B (de)	1980-02-11
US4148901A (en)	1979-04-10
NL7613166A (nl)	1977-05-27
FR2339599B1 (de)	1982-03-26
FR2333783A1 (fr)	1977-07-01
JPS5265244A (en)	1977-05-30
DE2652451A1 (de)	1977-06-08
DD129283A5 (de)	1978-01-11

Legal Events

Date	Code	Title	Description
1983-07-29	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
FR2521141A1 (fr)	1983-08-12	Nouveaux derives du cyano-2 benzimidazole, leur preparation et leur utilisation comme fongicides
BE529063A (de)
EP0335806B1 (de)	1995-11-02	Beta-Phenoxynitril-Verbindungen
CH427400A (fr)	1966-12-31	Composition fongicide
BE886128A (fr)	1981-05-13	Nouveaux derives du 1,2,4-triazole, leur preparation et leur utilisation comme agents fongicides
US4148901A (en)	1979-04-10	N-phenyl or n-pyridyl sulfamides and methanesulfonamides
FR2622582A1 (fr)	1989-05-05	Composes a groupe imidazole ou triazole, utilisation de ceux-ci a titre de fongicide, procede de preparation
US4219558A (en)	1980-08-26	Organic fluoro-imides and their use as miticides, etc.
BE886127A (fr)	1981-05-13	Nouveaux derives de l'imidazole, leur preparation et leur application comme agents fongicides
EP0017602A1 (de)	1980-10-15	2-Phenyl-4-pyron-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
US4282241A (en)	1981-08-04	Organic fluoro-imides, their preparation and use
FR2745469A1 (fr)	1997-09-05	Pyrazoles fongicides
LU85259A1 (fr)	1985-10-14	Ester de l'hydroxyde de tricyclohexyletain acaricide
EP0246171A2 (de)	1987-11-19	Fungizide Zusammensetzungen, die Nikotinsäurederivate enthalten, Nikotinsäurederivate und ihre Herstellung
BE826376A (fr)	1975-09-08	Dinitroanilines
US4085220A (en)	1978-04-18	2-Alkenyl-N-[(trichloromethyl)thio]succinimides
CH642819A5 (en)	1984-05-15	Process for the agricultural production of ergot
FR2582307A1 (fr)	1986-11-28	Compose thiazolique, son procede de production, composition microbicide le contenant et ses applications
BE594942A (de)
FR2544587A1 (fr)	1984-10-26	Compositions fongicides contenant des 5-tertio-butyl-1,3,4-thiadiazole-2-yl-urees substituees
LU85451A1 (fr)	1985-04-17	Nouveaux derives de l'ethanol,leur preparation et leur utilisation comme fongicides
EP0316245A1 (de)	1989-05-17	Fungizide Nicotinsäurederivate
FR2492820A1 (fr)	1982-04-30	Nouveaux derives oxime, procede pour leur preparation et leur application comme agents microbicides
CH635325A5 (en)	1983-03-31	Fungicidal complex compound
BE705793A (de)	1968-04-29