IL32561A - Preparation of thionothiol-phosphoric acid o,s-diester amides and their use as pesticides - Google Patents
Preparation of thionothiol-phosphoric acid o,s-diester amides and their use as pesticidesInfo
- Publication number
- IL32561A IL32561A IL32561A IL3256169A IL32561A IL 32561 A IL32561 A IL 32561A IL 32561 A IL32561 A IL 32561A IL 3256169 A IL3256169 A IL 3256169A IL 32561 A IL32561 A IL 32561A
- Authority
- IL
- Israel
- Prior art keywords
- diester
- radical
- active compound
- denotes
- alkyl
- Prior art date
Links
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 title claims description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 title claims description 3
- 238000002360 preparation method Methods 0.000 title description 13
- 239000000575 pesticide Substances 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 88
- -1 alkenyl radicals Chemical class 0.000 claims description 65
- 238000000034 method Methods 0.000 claims description 44
- 239000002253 acid Substances 0.000 claims description 31
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 18
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- 238000006243 chemical reaction Methods 0.000 claims description 14
- 230000006378 damage Effects 0.000 claims description 13
- 125000005843 halogen group Chemical group 0.000 claims description 13
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- 125000003545 alkoxy group Chemical group 0.000 claims description 11
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
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- RMRFFCXPLWYOOY-UHFFFAOYSA-N allyl radical Chemical compound [CH2]C=C RMRFFCXPLWYOOY-UHFFFAOYSA-N 0.000 claims description 2
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- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 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
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 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
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000005309 thioalkoxy group Chemical group 0.000 description 1
- 150000003573 thiols Chemical group 0.000 description 1
- WQYSXVGEZYESBR-UHFFFAOYSA-N thiophosphoryl chloride Chemical compound ClP(Cl)(Cl)=S WQYSXVGEZYESBR-UHFFFAOYSA-N 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 150000003738 xylenes Chemical class 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
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19681793118 DE1793118C3 (de) | 1968-08-05 | Thionothiolphosphorsäure-O.S-diesteramide und Verfahren zu deren Herstellung |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL32561A0 IL32561A0 (en) | 1969-09-25 |
| IL32561A true IL32561A (en) | 1972-12-29 |
Family
ID=5707582
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL32561A IL32561A (en) | 1968-08-05 | 1969-07-07 | Preparation of thionothiol-phosphoric acid o,s-diester amides and their use as pesticides |
Country Status (11)
| Country | Link |
|---|---|
| AT (1) | AT291294B (de) |
| BE (1) | BE737117A (de) |
| CH (1) | CH515936A (de) |
| CS (1) | CS153048B2 (de) |
| ES (1) | ES370202A1 (de) |
| FR (1) | FR2015096A1 (de) |
| GB (1) | GB1263513A (de) |
| IL (1) | IL32561A (de) |
| NL (1) | NL162078C (de) |
| PL (1) | PL83177B1 (de) |
| RO (1) | RO57378A (de) |
-
1969
- 1969-07-04 CH CH1026869A patent/CH515936A/de not_active IP Right Cessation
- 1969-07-07 IL IL32561A patent/IL32561A/en unknown
- 1969-07-24 RO RO60621A patent/RO57378A/ro unknown
- 1969-07-28 AT AT726069A patent/AT291294B/de not_active IP Right Cessation
- 1969-07-31 GB GB38428/69A patent/GB1263513A/en not_active Expired
- 1969-08-04 CS CS539669A patent/CS153048B2/cs unknown
- 1969-08-04 ES ES370202A patent/ES370202A1/es not_active Expired
- 1969-08-04 PL PL1969135224A patent/PL83177B1/pl unknown
- 1969-08-05 FR FR6926881A patent/FR2015096A1/fr not_active Withdrawn
- 1969-08-05 NL NL6911925.A patent/NL162078C/xx not_active IP Right Cessation
- 1969-08-05 BE BE737117D patent/BE737117A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB1263513A (en) | 1972-02-09 |
| NL162078C (nl) | 1980-04-15 |
| ES370202A1 (es) | 1971-04-01 |
| PL83177B1 (de) | 1975-12-31 |
| NL162078B (nl) | 1979-11-15 |
| DE1793118B2 (de) | 1976-11-18 |
| NL6911925A (de) | 1970-02-09 |
| BE737117A (de) | 1970-02-05 |
| RO57378A (de) | 1975-02-15 |
| AT291294B (de) | 1971-07-12 |
| IL32561A0 (en) | 1969-09-25 |
| CH515936A (de) | 1971-11-30 |
| CS153048B2 (de) | 1974-02-22 |
| DE1793118A1 (de) | 1972-02-24 |
| FR2015096A1 (de) | 1970-04-24 |
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