DD143848A5 - Mittel zur bekaempfung von pilzen - Google Patents
Mittel zur bekaempfung von pilzen Download PDFInfo
- Publication number
- DD143848A5 DD143848A5 DD79212873A DD21287379A DD143848A5 DD 143848 A5 DD143848 A5 DD 143848A5 DD 79212873 A DD79212873 A DD 79212873A DD 21287379 A DD21287379 A DD 21287379A DD 143848 A5 DD143848 A5 DD 143848A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- formula
- halogen
- methyl
- alkyl
- hydrogen
- Prior art date
Links
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 15
- 241000233866 Fungi Species 0.000 claims abstract description 14
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 14
- 150000002367 halogens Chemical class 0.000 claims abstract description 14
- 239000001257 hydrogen Substances 0.000 claims abstract description 14
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 7
- 150000002431 hydrogen Chemical group 0.000 claims abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 5
- 230000003032 phytopathogenic effect Effects 0.000 claims abstract description 4
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 3
- 125000001424 substituent group Chemical group 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 36
- 239000000203 mixture Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 10
- 239000000460 chlorine Substances 0.000 claims description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
- 229910052801 chlorine Inorganic materials 0.000 claims description 6
- -1 1 -methoxycarbonyl-ethyl Chemical group 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 abstract description 23
- 239000002855 microbicide agent Substances 0.000 abstract description 9
- 125000003545 alkoxy group Chemical group 0.000 abstract description 3
- 238000003898 horticulture Methods 0.000 abstract description 2
- XSQGPOLQOVDTBN-UHFFFAOYSA-N 2-hydrazinyl-n-phenylacetamide Chemical class NNCC(=O)NC1=CC=CC=C1 XSQGPOLQOVDTBN-UHFFFAOYSA-N 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 description 29
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
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- 239000000126 substance Substances 0.000 description 10
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
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- 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 6
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- 244000105624 Arachis hypogaea Species 0.000 description 3
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- 206010017533 Fungal infection Diseases 0.000 description 3
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
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- 241000233622 Phytophthora infestans Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
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- RHUYHJGZWVXEHW-UHFFFAOYSA-N 1,1-Dimethyhydrazine Chemical compound CN(C)N RHUYHJGZWVXEHW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 235000004535 Avena sterilis Nutrition 0.000 description 2
- 241001647031 Avena sterilis Species 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- 240000008067 Cucumis sativus Species 0.000 description 2
- 235000009849 Cucumis sativus Nutrition 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 206010061217 Infestation Diseases 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 125000001980 alanyl group Chemical group 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 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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- SRAWNDFHGTVUNZ-UHFFFAOYSA-M sodium;3,6-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(CCCC)=CC2=CC(CCCC)=CC=C21 SRAWNDFHGTVUNZ-UHFFFAOYSA-M 0.000 description 2
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- HNCCKHGOWJUHJZ-UHFFFAOYSA-N methyl 2-(n-(2-chloroacetyl)-2,6-dimethylanilino)propanoate Chemical compound COC(=O)C(C)N(C(=O)CCl)C1=C(C)C=CC=C1C HNCCKHGOWJUHJZ-UHFFFAOYSA-N 0.000 description 1
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- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 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
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 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
- 150000003512 tertiary amines Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 229940072358 xylocaine Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/46—N-acyl derivatives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH546178A CH635313A5 (de) | 1978-05-19 | 1978-05-19 | Pflanzenmikrobizid wirkende hydrazino-acetanilid-derivate, verfahren zu ihrer herstellung sowie mikrobizide mittel mit diesen praeparaten als wirkstoffe. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD143848A5 true DD143848A5 (de) | 1980-09-17 |
Family
ID=4293986
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD79212873A DD143848A5 (de) | 1978-05-19 | 1979-05-14 | Mittel zur bekaempfung von pilzen |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US4207338A (en, 2012) |
| JP (1) | JPS54151925A (en, 2012) |
| AR (1) | AR225142A1 (en, 2012) |
| AT (1) | AT365038B (en, 2012) |
| AU (1) | AU521666B2 (en, 2012) |
| BE (1) | BE876358A (en, 2012) |
| CA (1) | CA1127178A (en, 2012) |
| CH (1) | CH635313A5 (en, 2012) |
| CS (1) | CS210688B2 (en, 2012) |
| DD (1) | DD143848A5 (en, 2012) |
| DE (1) | DE2919825A1 (en, 2012) |
| EG (1) | EG13669A (en, 2012) |
| FR (1) | FR2426043A1 (en, 2012) |
| GB (1) | GB2021110B (en, 2012) |
| IL (1) | IL57332A (en, 2012) |
| IT (1) | IT1114283B (en, 2012) |
| LU (1) | LU81282A1 (en, 2012) |
| NL (1) | NL7903901A (en, 2012) |
| NZ (1) | NZ190487A (en, 2012) |
| PH (1) | PH14955A (en, 2012) |
| PL (1) | PL116524B1 (en, 2012) |
| ZA (1) | ZA792441B (en, 2012) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH637368A5 (de) * | 1978-10-27 | 1983-07-29 | Ciba Geigy Ag | Anilinderivate und daraus hergestellte schaedlingsbekaempfungsmittel. |
| US4459227A (en) * | 1981-03-02 | 1984-07-10 | Duke University | Para-hydroxyphenylhydrazines as in situ precursors of iminoquinones and quinones |
| DE69108356T2 (de) * | 1990-11-17 | 1995-07-20 | Nihon Nohyaku Co Ltd | Hydrazonderivate, Verfahren zu ihrer Herstellung und ihre Verwendung. |
| US5753652A (en) * | 1991-07-03 | 1998-05-19 | Novartis Corporation | Antiretroviral hydrazine derivatives |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3780095A (en) * | 1970-04-08 | 1973-12-18 | Byk Gulden Lomberg Chem Fab | Acylated anilino-carboxylic acids and their salts |
| US4151299A (en) * | 1974-04-09 | 1979-04-24 | Ciba-Geigy Corporation | Certain aniline derivatives as microbicidal agents |
| US4093738A (en) * | 1974-04-09 | 1978-06-06 | Ciba-Geigy Corporation | Microbicidally-active acylated anilino-carboxylic acid esters and their compositions |
| OA04979A (fr) * | 1974-04-09 | 1980-11-30 | Ciba Geigy | Nouveaux dérivés de l'aniline utiles comme agents microbicides et leur procédé de préparation. |
-
1978
- 1978-05-19 CH CH546178A patent/CH635313A5/de not_active IP Right Cessation
-
1979
- 1979-05-11 US US06/039,011 patent/US4207338A/en not_active Expired - Lifetime
- 1979-05-14 DD DD79212873A patent/DD143848A5/de not_active IP Right Cessation
- 1979-05-15 PL PL1979215594A patent/PL116524B1/pl unknown
- 1979-05-16 FR FR7912405A patent/FR2426043A1/fr active Granted
- 1979-05-16 DE DE19792919825 patent/DE2919825A1/de active Granted
- 1979-05-16 EG EG294/79A patent/EG13669A/xx active
- 1979-05-17 GB GB7917290A patent/GB2021110B/en not_active Expired
- 1979-05-17 AR AR276564A patent/AR225142A1/es active
- 1979-05-17 CS CS793432A patent/CS210688B2/cs unknown
- 1979-05-17 NL NL7903901A patent/NL7903901A/xx not_active Application Discontinuation
- 1979-05-17 LU LU81282A patent/LU81282A1/de unknown
- 1979-05-17 CA CA327,830A patent/CA1127178A/en not_active Expired
- 1979-05-18 IL IL57332A patent/IL57332A/xx unknown
- 1979-05-18 AT AT0369479A patent/AT365038B/de not_active IP Right Cessation
- 1979-05-18 IT IT22835/79A patent/IT1114283B/it active
- 1979-05-18 ZA ZA792441A patent/ZA792441B/xx unknown
- 1979-05-18 PH PH22516A patent/PH14955A/en unknown
- 1979-05-18 NZ NZ190487A patent/NZ190487A/xx unknown
- 1979-05-18 BE BE0/195238A patent/BE876358A/xx not_active IP Right Cessation
- 1979-05-18 AU AU47191/79A patent/AU521666B2/en not_active Ceased
- 1979-05-19 JP JP6213179A patent/JPS54151925A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| IL57332A (en) | 1982-11-30 |
| IT1114283B (it) | 1986-01-27 |
| AT365038B (de) | 1981-12-10 |
| CH635313A5 (de) | 1983-03-31 |
| US4207338A (en) | 1980-06-10 |
| LU81282A1 (de) | 1979-12-07 |
| JPS54151925A (en) | 1979-11-29 |
| NL7903901A (nl) | 1979-11-21 |
| FR2426043A1 (fr) | 1979-12-14 |
| JPS6320814B2 (en, 2012) | 1988-04-30 |
| PH14955A (en) | 1982-02-02 |
| ATA369479A (de) | 1981-05-15 |
| BE876358A (fr) | 1979-11-19 |
| CA1127178A (en) | 1982-07-06 |
| AU521666B2 (en) | 1982-04-22 |
| GB2021110B (en) | 1982-10-20 |
| IT7922835A0 (it) | 1979-05-18 |
| GB2021110A (en) | 1979-11-28 |
| PL215594A1 (en, 2012) | 1980-02-11 |
| PL116524B1 (en) | 1981-06-30 |
| FR2426043B1 (en, 2012) | 1983-12-16 |
| AR225142A1 (es) | 1982-02-26 |
| EG13669A (en) | 1982-03-31 |
| ZA792441B (en) | 1980-06-25 |
| AU4719179A (en) | 1979-11-22 |
| DE2919825C2 (en, 2012) | 1988-09-01 |
| CS210688B2 (en) | 1982-01-29 |
| NZ190487A (en) | 1981-10-19 |
| IL57332A0 (en) | 1979-09-30 |
| DE2919825A1 (de) | 1979-11-22 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ENJ | Ceased due to non-payment of renewal fee |