GB795860A - Sulphoxide-containing esters of phosphoric, thiophosphoric and phosphonic acids - Google Patents
Sulphoxide-containing esters of phosphoric, thiophosphoric and phosphonic acidsInfo
- Publication number
- GB795860A GB795860A GB31384/55A GB3138455A GB795860A GB 795860 A GB795860 A GB 795860A GB 31384/55 A GB31384/55 A GB 31384/55A GB 3138455 A GB3138455 A GB 3138455A GB 795860 A GB795860 A GB 795860A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl radicals
- substituted alkyl
- esters
- alkoxy
- radicals
- 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
- 150000002148 esters Chemical class 0.000 title abstract 4
- ATTZFSUZZUNHBP-UHFFFAOYSA-N Piperonyl sulfoxide Chemical compound CCCCCCCCS(=O)C(C)CC1=CC=C2OCOC2=C1 ATTZFSUZZUNHBP-UHFFFAOYSA-N 0.000 title 1
- 150000003009 phosphonic acids Chemical class 0.000 title 1
- 150000003016 phosphoric acids Chemical class 0.000 title 1
- 150000003582 thiophosphoric acids Chemical class 0.000 title 1
- -1 alkylene radical Chemical group 0.000 abstract 9
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 4
- 239000007858 starting material Substances 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 150000005840 aryl radicals Chemical class 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 150000003580 thiophosphoric acid esters Chemical class 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 abstract 1
- 229960000583 acetic acid Drugs 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000004965 chloroalkyl group Chemical group 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 239000012362 glacial acetic acid Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 150000003014 phosphoric acid esters Chemical class 0.000 abstract 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052698 phosphorus Inorganic materials 0.000 abstract 1
- 239000011574 phosphorus Substances 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- 230000009885 systemic effect Effects 0.000 abstract 1
- 150000003568 thioethers Chemical class 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
- C07F9/091—Esters of phosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
-
- 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
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/1651—Esters of thiophosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
-
- 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE338442X | 1954-11-06 | ||
| DEF21822A DE1039511B (de) | 1954-11-06 | 1954-11-06 | Verfahren zur Herstellung von Sulfoxydgruppen enthaltenden Estern der Phosphor- und Thiophosphorsaeuren |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB795860A true GB795860A (en) | 1958-05-28 |
Family
ID=25817297
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB31384/55A Expired GB795860A (en) | 1954-11-06 | 1955-11-02 | Sulphoxide-containing esters of phosphoric, thiophosphoric and phosphonic acids |
| GB35440/57A Expired GB834354A (en) | 1954-11-06 | 1957-11-13 | Esters of thiophosphoric acids containing sulphoxide groups |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB35440/57A Expired GB834354A (en) | 1954-11-06 | 1957-11-13 | Esters of thiophosphoric acids containing sulphoxide groups |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US2963505A (en, 2012) |
| BE (2) | BE561989A (en, 2012) |
| CH (2) | CH338442A (en, 2012) |
| DE (1) | DE1039511B (en, 2012) |
| FR (1) | FR1138426A (en, 2012) |
| GB (2) | GB795860A (en, 2012) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT559812A (en, 2012) * | 1954-08-02 | |||
| DE1083811B (de) * | 1958-11-07 | 1960-06-23 | Bayer Ag | Verfahren zur Herstellung von Benzylthiomethylaetherthiophosphor-verbindungen |
| NL250415A (en, 2012) * | 1959-04-13 | |||
| US3112269A (en) * | 1960-12-23 | 1963-11-26 | Shell Oil Co | Lubricating compositions containing sulfoxy alkyl phosphono compounds |
| CH387622A (de) * | 1959-10-09 | 1965-02-15 | Bayer Ag | Verfahren zur Herstellung von Thionophosphonsäureestern |
| US3223754A (en) * | 1959-12-04 | 1965-12-14 | Bayer Ag | Alkyl mercapto alkyl esters of substituted phosphonic acids |
| GB967627A (en) * | 1959-12-14 | 1964-08-26 | Shell Int Research | Thiophosphonic acid derivatives and compositions containing them |
| US3151147A (en) * | 1961-10-12 | 1964-09-29 | Shell Oil Co | Omicron, omicron-dialkyl omicron-1-sulfonylvinyl and omicron, omicron-dialkyl omicron-1-sulfinylvinyl phosphates |
| US3126314A (en) * | 1961-10-18 | 1964-03-24 | S-chlorophenylsblfonylmethyl - o | |
| US3228999A (en) * | 1962-06-11 | 1966-01-11 | Bayer Ag | Alkoxy carbonyl, amino carbonyl and cyano derivatives of alkyl or aryl mercapto, sulphono or sulphoxido ethyl esters of thio-phosphorus acids |
| US3246052A (en) * | 1962-12-26 | 1966-04-12 | Universal Oil Prod Co | Halogenated aromatic phosphate esters |
| US3925516A (en) * | 1973-04-02 | 1975-12-09 | American Cyanamid Co | S-({60 -Substituted-arylmethylthio, -arylmethylsulfinyl, and -arylmethylsulfonyl)methylphosphorus esters |
| US3939263A (en) * | 1973-05-09 | 1976-02-17 | American Cyanamid Company | Methods of combatting insects and acarina using oxygenated derivatives of S-(tert-bulythio)methyl O,O-diethyl phosphorodithioate and phosphorothioate |
| US3878267A (en) * | 1973-05-09 | 1975-04-15 | American Cyanamid Co | Oxygenated derivatives of s-(tert-butylthio)methyl o,o-diethyl phosphorodithioate and phosphorothioate |
| US4000269A (en) * | 1974-04-05 | 1976-12-28 | American Cyanamid Company | S-(α-substituted-arylmethylthio, -arylmethylsulfinyl, and -arylmethylsulfonyl)methyl phosphorus esters used as insecticides |
| US5635449A (en) * | 1995-04-07 | 1997-06-03 | American Cyanamid Company | Arylthioalkyl- and arylthioalkenylphosphonic acids and derivatives thereof useful as herbicidal agents |
| CN102395271A (zh) | 2009-03-25 | 2012-03-28 | 拜尔农作物科学股份公司 | 具有杀虫和杀螨特性的活性化合物结合物 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE830508C (de) * | 1950-05-24 | 1952-02-04 | Bayer Ag | Verfahren zur Herstellung von neutralen Estern der Thiophosphorsaeure |
| DE876691C (de) * | 1951-07-06 | 1953-05-18 | Bayer Ag | Verfahren zur Herstellung von Dithiophosphorsaeureestern |
| DE876692C (de) * | 1951-07-07 | 1953-05-18 | Bayer Ag | Verfahren zur Herstellung von Thiophosphorsaeureestern |
| DE871448C (de) * | 1951-07-31 | 1953-03-23 | Bayer Ag | Verfahren zur Herstellung von Estern der Monothiophosphorsaeure |
| NL184060B (nl) * | 1952-12-31 | Basf Ag | Werkwijze voor het opwerken van cyclohexanol en cyclohexanon bevattende reactiemengsels. | |
| DE947368C (de) * | 1954-11-06 | 1956-08-16 | Bayer Ag | Verfahren zur Herstellung von Sulfoxydgruppen enthaltenden Estern der Phosphor- und Thiophosphorsaeuren |
-
0
- BE BE542600D patent/BE542600A/xx unknown
- BE BE561989D patent/BE561989A/xx unknown
-
1954
- 1954-11-06 DE DEF21822A patent/DE1039511B/de active Pending
-
1955
- 1955-10-12 CH CH338442D patent/CH338442A/de unknown
- 1955-11-02 GB GB31384/55A patent/GB795860A/en not_active Expired
- 1955-11-05 FR FR1138426D patent/FR1138426A/fr not_active Expired
-
1957
- 1957-03-14 US US645913A patent/US2963505A/en not_active Expired - Lifetime
- 1957-10-17 CH CH361799D patent/CH361799A/de unknown
- 1957-11-13 GB GB35440/57A patent/GB834354A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB834354A (en) | 1960-05-04 |
| DE1039511B (de) | 1958-09-25 |
| US2963505A (en) | 1960-12-06 |
| CH338442A (de) | 1959-05-31 |
| FR1138426A (fr) | 1957-06-13 |
| BE561989A (en, 2012) | |
| BE542600A (en, 2012) | |
| CH361799A (de) | 1962-05-15 |
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