GB861402A - Organic phosphoramidates - Google Patents
Organic phosphoramidatesInfo
- Publication number
- GB861402A GB861402A GB1573/59A GB157359A GB861402A GB 861402 A GB861402 A GB 861402A GB 1573/59 A GB1573/59 A GB 1573/59A GB 157359 A GB157359 A GB 157359A GB 861402 A GB861402 A GB 861402A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- phosphoramidate
- methyl
- formula
- active ingredient
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 150000008298 phosphoramidates Chemical class 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 abstract 3
- 241001465754 Metazoa Species 0.000 abstract 3
- 239000004480 active ingredient Substances 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 abstract 2
- -1 4 - tertiary - butyl - 2 - chlorophenyl methyl methyl Chemical group 0.000 abstract 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 abstract 2
- 229910021529 ammonia Inorganic materials 0.000 abstract 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 244000045947 parasite Species 0.000 abstract 2
- 230000000361 pesticidal effect Effects 0.000 abstract 2
- PTMHPRAIXMAOOB-UHFFFAOYSA-L phosphoramidate Chemical compound NP([O-])([O-])=O PTMHPRAIXMAOOB-UHFFFAOYSA-L 0.000 abstract 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 abstract 2
- 239000000047 product Substances 0.000 abstract 2
- 230000009885 systemic effect Effects 0.000 abstract 2
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 abstract 1
- 239000001828 Gelatine Substances 0.000 abstract 1
- OHPFWWFHZGSBJB-UHFFFAOYSA-N N-[(2-chloro-4-propan-2-ylphenoxy)-ethoxyphosphoryl]methanamine Chemical compound CNP(OC1=C(C=C(C=C1)C(C)C)Cl)(OCC)=O OHPFWWFHZGSBJB-UHFFFAOYSA-N 0.000 abstract 1
- 239000002671 adjuvant Substances 0.000 abstract 1
- 150000003973 alkyl amines Chemical class 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 239000002775 capsule Substances 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 239000012141 concentrate Substances 0.000 abstract 1
- 235000008504 concentrate Nutrition 0.000 abstract 1
- WVPKAWVFTPWPDB-UHFFFAOYSA-M dichlorophosphinate Chemical compound [O-]P(Cl)(Cl)=O WVPKAWVFTPWPDB-UHFFFAOYSA-M 0.000 abstract 1
- WVPKAWVFTPWPDB-UHFFFAOYSA-N dichlorophosphinic acid Chemical class OP(Cl)(Cl)=O WVPKAWVFTPWPDB-UHFFFAOYSA-N 0.000 abstract 1
- 239000002270 dispersing agent Substances 0.000 abstract 1
- 239000008157 edible vegetable oil Substances 0.000 abstract 1
- 229920000159 gelatin Polymers 0.000 abstract 1
- 235000019322 gelatine Nutrition 0.000 abstract 1
- 230000002363 herbicidal effect Effects 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 238000010255 intramuscular injection Methods 0.000 abstract 1
- 239000007927 intramuscular injection Substances 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 229910001629 magnesium chloride Inorganic materials 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 235000020786 mineral supplement Nutrition 0.000 abstract 1
- QSXWTGFXQDSZDO-UHFFFAOYSA-N n-[[2-chloro-4-(2-methylbutan-2-yl)phenoxy]-methoxyphosphoryl]methanamine Chemical compound CCC(C)(C)C1=CC=C(OP(=O)(NC)OC)C(Cl)=C1 QSXWTGFXQDSZDO-UHFFFAOYSA-N 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 230000000590 parasiticidal effect Effects 0.000 abstract 1
- 239000008188 pellet Substances 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 235000020183 skimmed milk Nutrition 0.000 abstract 1
- 239000007921 spray Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 235000020357 syrup Nutrition 0.000 abstract 1
- 239000006188 syrup Substances 0.000 abstract 1
- 235000019195 vitamin supplement Nutrition 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000004563 wettable powder Substances 0.000 abstract 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
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/14—Esters of phosphoric acids containing P(=O)-halide groups
- C07F9/1406—Esters of phosphoric acids containing P(=O)-halide groups containing the structure Hal-P(=O)-O-aryl
-
- 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
- C07F9/2404—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/242—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic of hydroxyaryl compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US750103A US2929762A (en) | 1958-07-22 | 1958-07-22 | Phosphoramidates |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB861402A true GB861402A (en) | 1961-02-22 |
Family
ID=25016512
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1573/59A Expired GB861402A (en) | 1958-07-22 | 1959-01-15 | Organic phosphoramidates |
Country Status (7)
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1224312B (de) * | 1960-04-22 | 1966-09-08 | Dow Chemical Co | Verfahren zur Herstellung von Phosphorsaeure-O-chlorphenyl-O-alkylesteramiden |
| US3162575A (en) * | 1961-12-04 | 1964-12-22 | Consumers Cooperative Ass | Method of controlling face flies on livestock |
| US3166472A (en) * | 1962-01-12 | 1965-01-19 | Shell Oil Co | Anthelmintic compositions and method of employing same |
| BE629625A (US07935154-20110503-C00006.png) * | 1962-03-15 | |||
| US3212967A (en) * | 1962-11-05 | 1965-10-19 | Dow Chemical Co | Biocidally-active mixed phosphorothioate ester-containing and mixed phosphoramidate ester-containing polymeric materials |
| CH471156A (de) * | 1965-11-23 | 1969-04-15 | Sandoz Ag | Verfahren zur Herstellung von Phosphorsäurederivaten und Verwendung derselben zur Schädlingsbekämpfung |
| US3475536A (en) * | 1967-06-01 | 1969-10-28 | Dow Chemical Co | Method for the systemic control of ectoparasites with phosphorodiamidates |
| US3511632A (en) * | 1967-08-04 | 1970-05-12 | Ethyl Corp | Herbicidal organophosphorus-nitrogen compositions and method using same |
| US4380537A (en) * | 1977-11-21 | 1983-04-19 | The Dow Chemical Company | Stabilized insecticide formulations |
| US5958905A (en) * | 1996-03-26 | 1999-09-28 | Texas Biotechnology Corporation | Phosphoramidates, phosphinic amides and related compounds and the use thereof to modulate the activity of endothelin |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1869768A (en) * | 1928-11-22 | 1932-08-02 | Ig Farbenindustrie Ag | Production of phosphoric esters |
| US2033918A (en) * | 1934-03-22 | 1936-03-17 | Dow Chemical Co | Liquid organo derivatives of phosphoric acid |
| US2506344A (en) * | 1948-03-09 | 1950-05-02 | Piant Products Corp | Method for making thiophosphates |
| US2552540A (en) * | 1949-04-15 | 1951-05-15 | Dow Chemical Co | O-methoxy o-alkyl amidothiophosphates |
| US2552541A (en) * | 1949-06-09 | 1951-05-15 | Dow Chemical Co | O-(halophenyl) o-alkyl amidothiophosphates |
| DE823293C (de) * | 1950-02-23 | 1951-12-03 | Farbwerke Hoechst Vormals Meis | Verfahren zur Herstellung organischer, chlorhaltiger Phosphorsaeureabkoemmlinge |
| US2852469A (en) * | 1955-01-07 | 1958-09-16 | Inst Francais Du Petrole | Hydrocarbon-soluble molybdenum blues |
| NL96365C (US07935154-20110503-C00006.png) * | 1956-04-02 | |||
| US2855425A (en) * | 1956-04-04 | 1958-10-07 | Dow Chemical Co | O-(2, 6-dicyclohexyl-4-methylphenyl) o-methyl n-alkyl phosphoroamidothioates |
| US2831015A (en) * | 1956-04-30 | 1958-04-15 | Dow Chemical Co | O-(chlorophenyl) o-(chlorophenoxy-ethyl) phosphorothioates |
-
0
- LU LU37845D patent/LU37845A1/xx unknown
- NL NL239750D patent/NL239750A/xx unknown
- NL NL120405D patent/NL120405C/xx active
-
1958
- 1958-07-22 US US750103A patent/US2929762A/en not_active Expired - Lifetime
-
1959
- 1959-01-15 GB GB1573/59A patent/GB861402A/en not_active Expired
- 1959-05-29 DE DED39041A patent/DE1244779B/de active Pending
- 1959-05-29 DE DED30762A patent/DE1226362B/de active Pending
- 1959-06-01 CH CH7383459A patent/CH449321A/de unknown
- 1959-06-01 CH CH139564A patent/CH421101A/de unknown
- 1959-06-01 BE BE579237A patent/BE579237A/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL120405C (US07935154-20110503-C00006.png) | |
| DE1226362B (de) | 1966-10-06 |
| DE1244779B (de) | 1967-07-20 |
| NL239750A (US07935154-20110503-C00006.png) | |
| CH449321A (de) | 1967-12-31 |
| CH421101A (de) | 1966-09-30 |
| LU37845A1 (US07935154-20110503-C00006.png) | |
| BE579237A (fr) | 1959-12-01 |
| US2929762A (en) | 1960-03-22 |
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