IL28066A - Halogenated 2-hydroxy diphenyl-sulphones and microbicidal agents containing them - Google Patents

Halogenated 2-hydroxy diphenyl-sulphones and microbicidal agents containing them

Info

Publication number: IL28066A
Authority: IL; Israel
Prior art keywords: hydroxy; halogenated; atomic number; diphenyl; general formula
Prior art date: 1966-07-05

Application number

IL28066A

Other languages

English (en)

Original Assignee

Agripat 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.)

1966-07-05

Filing date

1967-05-29

Publication date

1971-02-25

1967-05-29 Application filed by Agripat Sa filed Critical Agripat Sa

1971-02-25 Publication of IL28066A publication Critical patent/IL28066A/en

Links

239000002855 microbicide agent Substances 0.000 title description 4
239000013543 active substance Substances 0.000 claims description 48
239000003795 chemical substances by application Substances 0.000 claims description 25
241000233866 Fungi Species 0.000 claims description 16
239000000969 carrier Substances 0.000 claims description 13
239000000203 mixture Substances 0.000 claims description 13
KZTYYGOKRVBIMI-UHFFFAOYSA-N S-phenyl benzenesulfonothioate Natural products C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 claims description 12
238000000034 method Methods 0.000 claims description 12
229910052736 halogen Inorganic materials 0.000 claims description 11
150000002367 halogens Chemical class 0.000 claims description 11
150000001875 compounds Chemical class 0.000 claims description 9
125000000217 alkyl group Chemical group 0.000 claims description 8
230000003641 microbiacidal effect Effects 0.000 claims description 8
241000894006 Bacteria Species 0.000 claims description 7
125000005843 halogen group Chemical group 0.000 claims description 7
239000000463 material Substances 0.000 claims description 7
244000005700 microbiome Species 0.000 claims description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical group OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 claims description 5
239000002253 acid Substances 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 4
239000011368 organic material Substances 0.000 claims description 4
230000003032 phytopathogenic effect Effects 0.000 claims description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
238000006243 chemical reaction Methods 0.000 claims description 3
239000000460 chlorine Substances 0.000 claims description 3
229910052801 chlorine Inorganic materials 0.000 claims description 3
150000008049 diazo compounds Chemical class 0.000 claims description 3
125000000018 nitroso group Chemical group N(=O)* 0.000 claims description 3
TWBPWBPGNQWFSJ-UHFFFAOYSA-N 2-phenylaniline Chemical group NC1=CC=CC=C1C1=CC=CC=C1 TWBPWBPGNQWFSJ-UHFFFAOYSA-N 0.000 claims description 2
150000007513 acids Chemical class 0.000 claims description 2
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244000046052 Phaseolus vulgaris Species 0.000 description 3
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239000000654 additive Substances 0.000 description 3
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ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
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150000002170 ethers Chemical class 0.000 description 2
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125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 2
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239000007858 starting material Substances 0.000 description 2
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235000011149 sulphuric acid Nutrition 0.000 description 2
238000010998 test method Methods 0.000 description 2
150000000183 1,3-benzoxazoles Chemical class 0.000 description 1
RZKKOBGFCAHLCZ-UHFFFAOYSA-N 1,4-dichloro-2-nitrobenzene Chemical compound [O-][N+](=O)C1=CC(Cl)=CC=C1Cl RZKKOBGFCAHLCZ-UHFFFAOYSA-N 0.000 description 1
JBWYXHHFYARVEZ-UHFFFAOYSA-N 1-chloro-3-nitrobenzene;sulfurochloridic acid Chemical compound OS(Cl)(=O)=O.[O-][N+](=O)C1=CC=CC(Cl)=C1 JBWYXHHFYARVEZ-UHFFFAOYSA-N 0.000 description 1
JCRNSBKSAQHNIN-UHFFFAOYSA-N 2,4-dibutylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(CCCC)=CC(CCCC)=C21 JCRNSBKSAQHNIN-UHFFFAOYSA-N 0.000 description 1
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
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LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Substances [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 1
VQTGUFBGYOIUFS-UHFFFAOYSA-N nitrosylsulfuric acid Chemical compound OS(=O)(=O)ON=O VQTGUFBGYOIUFS-UHFFFAOYSA-N 0.000 description 1
125000002811 oleoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
239000003973 paint Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
231100000208 phytotoxic Toxicity 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
235000019422 polyvinyl alcohol Nutrition 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
235000012219 potassium aluminium silicate Nutrition 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
235000012217 sodium aluminium silicate Nutrition 0.000 description 1
239000004289 sodium hydrogen sulphite Substances 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
150000003568 thioethers Chemical group 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
229960002447 thiram Drugs 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
239000011573 trace mineral Substances 0.000 description 1
PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/16—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C317/22—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C315/00—Preparation of sulfones; Preparation of sulfoxides
- C07C315/04—Preparation of sulfones; Preparation of sulfoxides by reactions not involving the formation of sulfone or sulfoxide groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

IL28066A 1966-07-05 1967-05-29 Halogenated 2-hydroxy diphenyl-sulphones and microbicidal agents containing them IL28066A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CH975966A CH483788A (de)	1966-07-05	1966-07-05	Mikrobiozides Mittel und dessen Verwendung
CH1551368A CH474492A (de)	1966-07-05	1966-07-05	Verfahren zur Herstellung von neuen Diphenylsulfonen

Publications (1)

Publication Number	Publication Date
IL28066A true IL28066A (en)	1971-02-25

Family

ID=25705277

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL28066A IL28066A (en)	1966-07-05	1967-05-29	Halogenated 2-hydroxy diphenyl-sulphones and microbicidal agents containing them

Country Status (6)

Country	Link
US (1)	US3551500A (de)
BE (1)	BE700913A (de)
CH (2)	CH483788A (de)
DE (1)	DE1287067B (de)
GB (1)	GB1136514A (de)
IL (1)	IL28066A (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3966817A (en) *	1974-03-25	1976-06-29	Shell Oil Company	Herbicidal ortho-nitroanilines
HU195951B (en) *	1984-02-29	1988-08-29	Richter Gedeon Vegyeszet	Process for producing amino-diaryl-sulfoxide derivatives and pharmaceutics comprising such compounds
JPS61130269A (ja) *	1984-11-30	1986-06-18	Kanzaki Paper Mfg Co Ltd	ヒドロキシジフエニルスルホン誘導体およびその誘導体を用いた感熱記録体

1966
- 1966-07-05 CH CH975966A patent/CH483788A/de not_active IP Right Cessation
- 1966-07-05 CH CH1551368A patent/CH474492A/de not_active IP Right Cessation
1967
- 1967-05-29 IL IL28066A patent/IL28066A/en unknown
- 1967-06-30 US US650189A patent/US3551500A/en not_active Expired - Lifetime
- 1967-07-04 DE DEA56172A patent/DE1287067B/de active Pending
- 1967-07-04 GB GB30718/67A patent/GB1136514A/en not_active Expired
- 1967-07-04 BE BE700913D patent/BE700913A/xx unknown

Also Published As

Publication number	Publication date
CH474492A (de)	1969-06-30
CH483788A (de)	1970-01-15
DE1287067B (de)	1969-01-16
GB1136514A (en)	1968-12-11
BE700913A (de)	1968-01-04
US3551500A (en)	1970-12-29

Publication	Publication Date	Title
JPH0625160B2 (ja)	1994-04-06	Ｎ−フエニルスルホニル−ｎ′−ピリミジニル尿素およびｎ−フエニルスルホニル−ｎ′−トリアジニル尿素、その製法並びに該化合物を含む植物の生長抑制剤
US3412149A (en)	1968-11-19	Phenyl-mercaptomethane-sulfonamide
IL28055A (en)	1971-06-23	Phenoxyalkyl(or phenylthioalkyl)trialkyl ammonium salts,their preparation and pesticidal compositions containing them
US2779788A (en)	1957-01-29	Trichloromethane sulphenic acid derivatives
US2806035A (en)	1957-09-10	Benztriazole derivatives
US3186904A (en)	1965-06-01	Fungicidal sulphones and sulphoxides
JPS58219149A (ja)	1983-12-20	アイオドプロパルギルアンモニウム塩類、それらの製造方法、および害虫防除剤としてのそれらの使用
US3551500A (en)	1970-12-29	2-hydroxy-4-halo-diphenyl sulfones
US2833689A (en)	1958-05-06	Fungicidal compositions comprising benzothiazole and benzoxazole carbonic acid estersand method of control of fungi
US2971884A (en)	1961-02-14	Method for the control of fungal organisms
IL25982A (en)	1970-03-22	5-sulphonyl-1,2-dithiol-3-one compounds,their preparation
US2839446A (en)	1958-06-17	New pyrimidine derivatives
US3562292A (en)	1971-02-09	N-substituted phthalimides
US3657437A (en)	1972-04-18	Agents inhibiting fungus growth and method of controlling fungi therewith
PL135140B1 (en)	1985-10-31	Pesticide and microbicide as well as method of obtainin halogen propargyloformamides
HU191074B (en)	1987-01-28	Fungicide and microbicide compositions containing n-sulfenilized benzyl-sulfonamides as active agents and process for producing the active agents
PL110797B1 (en)	1980-07-31	Fungicide
US2851391A (en)	1958-09-09	Processes and products
CH592411A5 (en)	1977-10-31	Phenoxymethyl- and phenylthiomethyl-pyridine derivs - with insecticidal, acaricidal and plant-growth regulating activity
US3707497A (en)	1972-12-26	Sulfonic acid cyanovinyl esters
US3636076A (en)	1972-01-18	N - fluorodichloromethylmercapto - n - trifluoromethyl - amino -benzoic acid phenyl esters
JPS6075450A (ja)	1985-04-27	ビスシクロヘキシルアミンアルカン及び該化合物を有効物質として含有する殺菌剤
US3692909A (en)	1972-09-19	Methods of combatting fungi using 6-alkylthio and 6-phenyl-thio pyrimidine derivatives
US2762740A (en)	1956-09-11	New acylated hydrazones and their use in the control of fungi
US2879198A (en)	1959-03-24	Trichloromethyl benzenethiosulfonates