CH638815A5 - N-((phosphinyl)-amino)-thio- und n-((phosphinothioyl)-amino)-thio-methylcarbamate, verfahren zu ihrer herstellung sowie ihre verwendung in pestiziden. - Google Patents
N-((phosphinyl)-amino)-thio- und n-((phosphinothioyl)-amino)-thio-methylcarbamate, verfahren zu ihrer herstellung sowie ihre verwendung in pestiziden. Download PDFInfo
- Publication number
- CH638815A5 CH638815A5 CH106979A CH106979A CH638815A5 CH 638815 A5 CH638815 A5 CH 638815A5 CH 106979 A CH106979 A CH 106979A CH 106979 A CH106979 A CH 106979A CH 638815 A5 CH638815 A5 CH 638815A5
- Authority
- CH
- Switzerland
- Prior art keywords
- radical
- methyl
- thio
- amino
- carbon atoms
- Prior art date
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- -1 (PHOSPHINYL) -AMINO Chemical class 0.000 title claims description 60
- 238000000034 method Methods 0.000 title claims description 11
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- 238000004519 manufacturing process Methods 0.000 title description 2
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- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 52
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 52
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 51
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 36
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims description 36
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- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- RJBIAAZJODIFHR-UHFFFAOYSA-N dihydroxy-imino-sulfanyl-$l^{5}-phosphane Chemical class NP(O)(O)=S RJBIAAZJODIFHR-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- HPYNZHMRTTWQTB-UHFFFAOYSA-N dimethylpyridine Natural products CC1=CC=CN=C1C HPYNZHMRTTWQTB-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 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 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 231100000418 oral toxicity Toxicity 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000012430 organic reaction media Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- 150000003012 phosphoric acid amides Chemical class 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000005080 plant death Effects 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 238000005549 size reduction Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 239000004455 soybean meal Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- 238000001363 water suppression through gradient tailored excitation Methods 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
- C07F9/2454—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic
- C07F9/2479—Compounds containing the structure P(=X)n-N-acyl, P(=X)n-N-heteroatom, P(=X)n-N-CN (X = O, S, Se; n = 0, 1)
- C07F9/2483—Compounds containing the structure P(=X)n-N-acyl, P(=X)n-N-heteroatom, P(=X)n-N-CN (X = O, S, Se; n = 0, 1) containing the structure P(=X)n-N-S (X = O, S, Se; n = 0, 1)
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus as a ring member
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
- C07F9/657154—Cyclic esteramides of oxyacids of phosphorus
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87495978A | 1978-02-03 | 1978-02-03 | |
| US05/962,266 US4208409A (en) | 1977-02-04 | 1978-11-20 | N-[(phosphinyl or phosphinothioyl)amino]thio-methylcarbamates and pesticidal methods |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH638815A5 true CH638815A5 (de) | 1983-10-14 |
Family
ID=27128362
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH106979A CH638815A5 (de) | 1978-02-03 | 1979-02-02 | N-((phosphinyl)-amino)-thio- und n-((phosphinothioyl)-amino)-thio-methylcarbamate, verfahren zu ihrer herstellung sowie ihre verwendung in pestiziden. |
Country Status (19)
| Country | Link |
|---|---|
| JP (1) | JPS5828879B2 (es) |
| AU (1) | AU521661B2 (es) |
| BR (1) | BR7900672A (es) |
| CA (1) | CA1133918A (es) |
| CH (1) | CH638815A5 (es) |
| DD (1) | DD141779A5 (es) |
| DE (1) | DE2902647A1 (es) |
| DK (1) | DK45379A (es) |
| EG (1) | EG14058A (es) |
| ES (1) | ES477417A1 (es) |
| FR (1) | FR2422673B1 (es) |
| GB (1) | GB2015527B (es) |
| HU (1) | HU184209B (es) |
| IL (1) | IL56502A (es) |
| IT (1) | IT1202876B (es) |
| NL (1) | NL7900857A (es) |
| OA (1) | OA06176A (es) |
| PL (1) | PL115203B1 (es) |
| YU (1) | YU24179A (es) |
-
1979
- 1979-01-24 DE DE19792902647 patent/DE2902647A1/de not_active Withdrawn
- 1979-01-24 AU AU43607/79A patent/AU521661B2/en not_active Ceased
- 1979-01-25 IL IL56502A patent/IL56502A/xx unknown
- 1979-02-02 BR BR7900672A patent/BR7900672A/pt unknown
- 1979-02-02 HU HU79UO153A patent/HU184209B/hu unknown
- 1979-02-02 DK DK45379A patent/DK45379A/da not_active Application Discontinuation
- 1979-02-02 YU YU00241/79A patent/YU24179A/xx unknown
- 1979-02-02 NL NL7900857A patent/NL7900857A/xx not_active Application Discontinuation
- 1979-02-02 CH CH106979A patent/CH638815A5/de not_active IP Right Cessation
- 1979-02-02 IT IT19865/79A patent/IT1202876B/it active
- 1979-02-02 ES ES477417A patent/ES477417A1/es not_active Expired
- 1979-02-02 FR FR7902723A patent/FR2422673B1/fr not_active Expired
- 1979-02-02 DD DD79210794A patent/DD141779A5/de unknown
- 1979-02-02 JP JP54011322A patent/JPS5828879B2/ja not_active Expired
- 1979-02-02 CA CA320,756A patent/CA1133918A/en not_active Expired
- 1979-02-02 GB GB7903755A patent/GB2015527B/en not_active Expired
- 1979-02-03 OA OA56726A patent/OA06176A/xx unknown
- 1979-02-03 PL PL1979213213A patent/PL115203B1/pl unknown
- 1979-02-03 EG EG69/79A patent/EG14058A/xx active
Also Published As
| Publication number | Publication date |
|---|---|
| FR2422673A1 (fr) | 1979-11-09 |
| HU184209B (en) | 1984-07-30 |
| GB2015527A (en) | 1979-09-12 |
| NL7900857A (nl) | 1979-08-07 |
| OA06176A (fr) | 1981-06-30 |
| EG14058A (en) | 1984-06-30 |
| GB2015527B (en) | 1982-04-21 |
| DK45379A (da) | 1979-08-04 |
| PL213213A1 (es) | 1980-02-25 |
| AU4360779A (en) | 1979-08-09 |
| YU24179A (en) | 1983-02-28 |
| PL115203B1 (en) | 1981-03-31 |
| DD141779A5 (de) | 1980-05-21 |
| IL56502A (en) | 1983-11-30 |
| FR2422673B1 (fr) | 1985-06-28 |
| JPS54115377A (en) | 1979-09-07 |
| AU521661B2 (en) | 1982-04-22 |
| IT7919865A0 (it) | 1979-02-02 |
| DE2902647A1 (de) | 1979-08-09 |
| CA1133918A (en) | 1982-10-19 |
| JPS5828879B2 (ja) | 1983-06-18 |
| BR7900672A (pt) | 1979-09-04 |
| ES477417A1 (es) | 1980-07-01 |
| IT1202876B (it) | 1989-02-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |