SU651643A3 - Средство дл борьбы с клещами - Google Patents
Средство дл борьбы с клещамиInfo
- Publication number
- SU651643A3 SU651643A3 SU731953836A SU1953836A SU651643A3 SU 651643 A3 SU651643 A3 SU 651643A3 SU 731953836 A SU731953836 A SU 731953836A SU 1953836 A SU1953836 A SU 1953836A SU 651643 A3 SU651643 A3 SU 651643A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- formamidine
- methyl
- hydrogen
- alkyl
- dimethyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title description 10
- 241000238876 Acari Species 0.000 title description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 8
- 230000000895 acaricidal effect Effects 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- PXXJHWLDUBFPOL-UHFFFAOYSA-N benzamidine Chemical class NC(=N)C1=CC=CC=C1 PXXJHWLDUBFPOL-UHFFFAOYSA-N 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 claims description 2
- 150000002431 hydrogen Chemical group 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 24
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 239000000243 solution Substances 0.000 description 14
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- -1 N-n-hexyl-N- (2,6-dimethylphenyl) -formamidine Chemical compound 0.000 description 9
- 238000001816 cooling Methods 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 239000005457 ice water Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- FOYHNROGBXVLLX-UHFFFAOYSA-N 2,6-diethylaniline Chemical compound CCC1=CC=CC(CC)=C1N FOYHNROGBXVLLX-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
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 238000005292 vacuum distillation Methods 0.000 description 3
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 description 2
- 239000000642 acaricide Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- MCZIJQYYIXXDDA-UHFFFAOYSA-N n-butyl-n-methylformamide Chemical compound CCCCN(C)C=O MCZIJQYYIXXDDA-UHFFFAOYSA-N 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- KWVPRPSXBZNOHS-UHFFFAOYSA-N 2,4,6-Trimethylaniline Chemical compound CC1=CC(C)=C(N)C(C)=C1 KWVPRPSXBZNOHS-UHFFFAOYSA-N 0.000 description 1
- WKBALTUBRZPIPZ-UHFFFAOYSA-N 2,6-di(propan-2-yl)aniline Chemical compound CC(C)C1=CC=CC(C(C)C)=C1N WKBALTUBRZPIPZ-UHFFFAOYSA-N 0.000 description 1
- 241001260012 Bursa Species 0.000 description 1
- 101000654316 Centruroides limpidus Beta-toxin Cll2 Proteins 0.000 description 1
- PNKUSGQVOMIXLU-UHFFFAOYSA-N Formamidine Chemical class NC=N PNKUSGQVOMIXLU-UHFFFAOYSA-N 0.000 description 1
- 241000193418 Paenibacillus larvae Species 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- HUMHYXGDUOGHTG-HEZXSMHISA-N alpha-D-GalpNAc-(1->3)-[alpha-L-Fucp-(1->2)]-D-Galp Chemical compound O[C@H]1[C@H](O)[C@H](O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](O[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](O)[C@@H](CO)OC1O HUMHYXGDUOGHTG-HEZXSMHISA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- KKEQDORUHMADQW-UHFFFAOYSA-N n,n-dimethyl-n'-(2,4,6-trimethylphenyl)methanimidamide Chemical compound CN(C)C=NC1=C(C)C=C(C)C=C1C KKEQDORUHMADQW-UHFFFAOYSA-N 0.000 description 1
- APVPOHHVBBYQAV-UHFFFAOYSA-N n-(4-aminophenyl)sulfonyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 APVPOHHVBBYQAV-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C257/00—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines
- C07C257/10—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines
- C07C257/18—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines having carbon atoms of amidino groups bound to carbon atoms of six-membered aromatic rings
-
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH473072A CH564304A5 (en) | 1972-03-29 | 1972-03-29 | Substd phenylformamidines |
| CH473172A CH564305A5 (en) | 1972-03-29 | 1972-03-29 | Substd phenylformamidines - acaricides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU651643A3 true SU651643A3 (ru) | 1979-03-05 |
Family
ID=25696154
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU731953836A SU651643A3 (ru) | 1972-03-29 | 1973-07-27 | Средство дл борьбы с клещами |
Country Status (19)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2234504C2 (ru) * | 1999-02-06 | 2004-08-20 | Авентис Кропсайенс Гмбх | Соединения, полезные в качестве фунгицидов, и способ уничтожения грибков |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4071556A (en) * | 1974-03-11 | 1978-01-31 | Stauffer Chemical Company | Formamidine insecticidal compounds |
| FI760163A7 (enrdf_load_stackoverflow) * | 1975-02-05 | 1976-08-06 | Huyck Corp | |
| JPS5516913A (en) * | 1978-07-18 | 1980-02-06 | Imaizumi Shigiyou Kk | Paper making blanket in paper making machine and production |
| EP0015440A1 (de) * | 1979-02-23 | 1980-09-17 | Hoechst Aktiengesellschaft | Substituierte N1-Vinyl-N1-methyl-N2-aryl-formamidine, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Schädlingsbekämpfungsmittel |
| CN111925303A (zh) * | 2020-08-12 | 2020-11-13 | 广东嘉博制药有限公司 | 一种盐酸罗哌卡因杂质的制备方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL253634A (enrdf_load_stackoverflow) * | 1959-07-10 | |||
| CH432929A (de) * | 1962-03-08 | 1967-03-31 | Ciba Geigy | Schädlingsbekämpfungsmittel |
| GB1212454A (en) * | 1967-03-04 | 1970-11-18 | Egyt Gyogyszervegyeszeti Gyar | N,n'-substituted formamidines |
-
1972
- 1972-03-28 BE BE129362A patent/BE797442A/xx unknown
-
1973
- 1973-03-19 IL IL41823A patent/IL41823A/en unknown
- 1973-03-21 CA CA166,698A patent/CA1051027A/en not_active Expired
- 1973-03-22 NL NL7304037A patent/NL7304037A/xx not_active Application Discontinuation
- 1973-03-23 US US344461A patent/US3929883A/en not_active Expired - Lifetime
- 1973-03-26 DE DE2315041A patent/DE2315041A1/de not_active Ceased
- 1973-03-27 AR AR247258A patent/AR217029A1/es active
- 1973-03-27 YU YU824/73A patent/YU36156B/xx unknown
- 1973-03-27 CS CS732224A patent/CS189605B2/cs unknown
- 1973-03-28 AT AT271173A patent/AT320611B/de not_active IP Right Cessation
- 1973-03-28 FR FR7311144A patent/FR2178117A1/fr not_active Withdrawn
- 1973-03-28 DD DD169789A patent/DD107907A5/xx unknown
- 1973-03-28 GB GB1493373A patent/GB1422216A/en not_active Expired
- 1973-03-28 IT IT22303/73A patent/IT988616B/it active
- 1973-03-28 ZA ZA732129A patent/ZA732129B/xx unknown
- 1973-03-29 BR BR732283A patent/BR7302283D0/pt unknown
- 1973-03-29 JP JP48036143A patent/JPS496124A/ja active Pending
- 1973-07-27 SU SU731953836A patent/SU651643A3/ru active
-
1979
- 1979-02-07 KE KE2917A patent/KE2917A/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2234504C2 (ru) * | 1999-02-06 | 2004-08-20 | Авентис Кропсайенс Гмбх | Соединения, полезные в качестве фунгицидов, и способ уничтожения грибков |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2178117A1 (enrdf_load_stackoverflow) | 1973-11-09 |
| KE2917A (en) | 1979-03-09 |
| CA1051027A (en) | 1979-03-20 |
| IT988616B (it) | 1975-04-30 |
| DD107907A5 (enrdf_load_stackoverflow) | 1974-08-20 |
| AU5368873A (en) | 1974-09-26 |
| US3929883A (en) | 1975-12-30 |
| DE2315041A1 (de) | 1973-10-11 |
| NL7304037A (enrdf_load_stackoverflow) | 1973-10-02 |
| GB1422216A (en) | 1976-01-21 |
| YU82473A (en) | 1981-06-30 |
| AR217029A1 (es) | 1980-02-29 |
| IL41823A0 (en) | 1973-05-31 |
| IL41823A (en) | 1977-12-30 |
| CS189605B2 (en) | 1979-04-30 |
| BE797442A (fr) | 1973-09-28 |
| BR7302283D0 (pt) | 1974-06-27 |
| AT320611B (de) | 1975-02-25 |
| YU36156B (en) | 1982-02-25 |
| JPS496124A (enrdf_load_stackoverflow) | 1974-01-19 |
| ZA732129B (en) | 1974-01-30 |
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