PL89021B1 - Fungicidal carboxylic acid nitriles[US3886283A] - Google Patents
Fungicidal carboxylic acid nitriles[US3886283A] Download PDFInfo
- Publication number
- PL89021B1 PL89021B1 PL1972155654A PL15565472A PL89021B1 PL 89021 B1 PL89021 B1 PL 89021B1 PL 1972155654 A PL1972155654 A PL 1972155654A PL 15565472 A PL15565472 A PL 15565472A PL 89021 B1 PL89021 B1 PL 89021B1
- Authority
- PL
- Poland
- Prior art keywords
- alpha
- measure according
- acid nitrile
- dimethoxyphenyl
- active ingredients
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/32—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Claims (8)
- Zastrzezenia patentowe 1. Srodek szkodnikobójczy, znamienny tym, ze zawiera jako substancje czynna 0,001-60% wa¬ gowych zwiazku o ogólnym wzorze 1, w którym R oznacza atom wodoru lub grupe alkilowa, zawierajaca 1—4 atomów wegla, R1 oznacza atom wodoru, grupe metylowa, grupe alkoksylowa, zawierajaca 1—4 atomów wegla lub ewentualnie podstawiona grupe fenylowa, R2 i R3 niezaleznie od siebie oznaczaja atom wodoru, grupe alkoksylowa, zawierajaca 1-4 atomów wegla, lub atom chlorowca, n oznacza liczbe calkowita 0-18 oraz obojetny, zazwyczaj uzywany do tego typu preparatów, staly lub ciekly nosnik lub rozcienczalnik.
- 2. Srodek wedlug zastrz. 1, znamienny tym, ze zawiera jako substancje czynna nitryl kwasu alfa-/3,4-dwumetoksyfenylo/-alfa-etylomaslowego.
- 3. Srodek wedlug zastrz. 1, znamienny tym, alfa-/3,4-dwumetoksyfenylo/-gamma-metoksymaslowego.
- 4. Srodek wedlug zastrz. 1, znamienny tym, alfa-/3,4-dwumetoksyfenylo/-walerianowego.
- 5. Srodek wedlug zastrz. 1, znamienny tym, alfa-/3,4-dwumetoksyfenylo/-beta-/-p-chlorofenylo/-propionowego.
- 6. Srodek wedlug zastrz. 1, znamienny tym, ze zawiera jako substancje czynna nitryl kwasu alfa-/p-chlorofenylo/-gamma-metoksymaslowego.
- 7. Srodek wedlug zastrz. 1, znamienny tym, ze zawiera jako substancje czynna nitryl kwasu alfa-/p-chlorofenylo/-walerianowego.
- 8. Srodek wedlug zastrz. 1, znamienny tym, ze zawiera jako substancje czynna nitryl kwasu alfa-/3,4-dwumetoksyfenylo/-stearynowego. ze zawiera jako substancje czynna nitryl kwasu ze zawiera jako substancje czynna nitryl kwasu ze zawiera jako substancje czynna nitryl kwasu89 021 R1—(Ob) r— (OfcJn—C—CN R3 R2 wzaR 1 CH2—CN W20R 2 PL
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HUCI1120A HU164015B (pl) | 1971-05-31 | 1971-05-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
PL89021B1 true PL89021B1 (en) | 1976-10-30 |
Family
ID=10994406
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL1972155654A PL89021B1 (en) | 1971-05-31 | 1972-05-29 | Fungicidal carboxylic acid nitriles[US3886283A] |
Country Status (15)
Country | Link |
---|---|
US (1) | US3886283A (pl) |
AT (1) | AT318300B (pl) |
AU (1) | AU4270772A (pl) |
BE (1) | BE784160A (pl) |
BR (1) | BR7203531D0 (pl) |
CA (1) | CA994239A (pl) |
CS (1) | CS196508B1 (pl) |
DD (1) | DD105381A1 (pl) |
DE (1) | DE2223957A1 (pl) |
ES (1) | ES403303A1 (pl) |
FR (1) | FR2143678B1 (pl) |
GB (1) | GB1386992A (pl) |
HU (1) | HU164015B (pl) |
IL (1) | IL39505A (pl) |
PL (1) | PL89021B1 (pl) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5163145A (en) * | 1974-11-26 | 1976-06-01 | Sumitomo Chemical Co | 33 mechiru 22 * 44 harogenofueniru * buchironitoriruno seizoho |
US4056509A (en) * | 1975-07-09 | 1977-11-01 | Shell Oil Company | Preparation of benzyl cyanides |
US4182625A (en) * | 1977-07-05 | 1980-01-08 | Stauffer Chemical Company | 3-Halo-5-(lower alkoxy) phenoxy alkyl amides |
US4224052A (en) * | 1978-05-05 | 1980-09-23 | American Cyanamid Company | Polysubstituted butanoic acids, esters and derivatives thereof utilizing the same as herbicides |
US4383848A (en) * | 1978-05-05 | 1983-05-17 | American Cyanamid Company | Polysubstituted butanoic acids, esters and derivatives thereof utilizing the same as herbicides |
US4430114A (en) | 1979-07-25 | 1984-02-07 | American Cyanamid Company | 2,6-Dinitroaniline herbicides, and use thereof |
DE3047106A1 (de) * | 1980-12-13 | 1982-07-29 | Henkel Kgaa | Topische kosmetische zubereitungen zur behandlung von stark fettendem haar und seborrhoeischer haut |
US4400204A (en) * | 1981-03-16 | 1983-08-23 | Stauffer Chemical Company | Substituted benzyloxy chloroethoxy ethane herbicide antidotes |
US4511394A (en) * | 1981-03-16 | 1985-04-16 | Stauffer Chemical Co. | Substituted benzyloxy chloroethoxy ethane herbicide antidotes |
US4489007A (en) * | 1981-03-16 | 1984-12-18 | Stauffer Chemical Company | Substituted benzyloxy chloroethoxy ethane herbicide antidotes |
JPS57185252A (en) * | 1981-05-07 | 1982-11-15 | Nippon Tokushu Kagaku Kogyo Kk | Production of phenylacetonitrile derivative |
US4806673A (en) * | 1986-12-10 | 1989-02-21 | The Dow Chemical Company | Preparation of cyanoalkylphenols from bisphenols |
US4916251A (en) * | 1987-01-02 | 1990-04-10 | The Dow Chemical Company | Cyanoisoalkylation of hydroxy substituted aryl compounds using ketones |
US7622504B2 (en) * | 2006-12-20 | 2009-11-24 | MCS Laboratories, Inc. | Esters of 2-phenylalkanenitriles and antifungal compositions containing them |
JP2020203835A (ja) * | 2017-08-25 | 2020-12-24 | アグロカネショウ株式会社 | フェニルアセトニトリル誘導体を用いた植物の細菌性病害の防除方法 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2695319A (en) * | 1954-11-23 | Process of producing verairyl | ||
US2740806A (en) * | 1953-01-29 | 1956-04-03 | Searle & Co | Nuclearly hydroxylated derivatives of alpha, beta-diphenylalkanonitriles |
US2897229A (en) * | 1954-02-09 | 1959-07-28 | Kali Chemie Ag | Phenyl acetonitrile compounds and a process of making same |
US3441617A (en) * | 1966-03-15 | 1969-04-29 | Lummus Co | Oxidation of aromatic compounds |
-
1971
- 1971-05-31 HU HUCI1120A patent/HU164015B/hu unknown
-
1972
- 1972-05-17 DE DE19722223957 patent/DE2223957A1/de active Pending
- 1972-05-23 IL IL39505A patent/IL39505A/en unknown
- 1972-05-24 US US256268A patent/US3886283A/en not_active Expired - Lifetime
- 1972-05-24 AT AT447472A patent/AT318300B/de not_active IP Right Cessation
- 1972-05-25 AU AU42707/72A patent/AU4270772A/en not_active Expired
- 1972-05-29 DD DD163260A patent/DD105381A1/xx unknown
- 1972-05-29 FR FR7219104A patent/FR2143678B1/fr not_active Expired
- 1972-05-29 PL PL1972155654A patent/PL89021B1/pl unknown
- 1972-05-30 BE BE784160A patent/BE784160A/xx not_active IP Right Cessation
- 1972-05-30 CS CS723717A patent/CS196508B1/cs unknown
- 1972-05-30 ES ES403303A patent/ES403303A1/es not_active Expired
- 1972-05-31 BR BR3531/72A patent/BR7203531D0/pt unknown
- 1972-05-31 CA CA143,542A patent/CA994239A/en not_active Expired
- 1972-05-31 GB GB2554272A patent/GB1386992A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR2143678B1 (pl) | 1975-03-28 |
DD105381A1 (pl) | 1974-04-20 |
FR2143678A1 (pl) | 1973-02-09 |
DE2223957A1 (de) | 1972-12-14 |
CA994239A (en) | 1976-08-03 |
AU4270772A (en) | 1973-11-29 |
BE784160A (fr) | 1972-09-18 |
GB1386992A (en) | 1975-03-12 |
HU164015B (pl) | 1973-12-28 |
BR7203531D0 (pt) | 1973-05-31 |
CS196508B1 (en) | 1980-03-31 |
US3886283A (en) | 1975-05-27 |
ES403303A1 (es) | 1975-05-01 |
IL39505A (en) | 1976-01-30 |
IL39505A0 (en) | 1972-09-28 |
AT318300B (de) | 1974-10-10 |
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