ES221370A1 - PROCEDIMIENTO DE FABRICACIoN DE NUEVOS ÉSTERES BáSICOS PESTICIDAS DE áCIDO FOSFOROTIOLOTIoNICO - Google Patents
PROCEDIMIENTO DE FABRICACIoN DE NUEVOS ÉSTERES BáSICOS PESTICIDAS DE áCIDO FOSFOROTIOLOTIoNICOInfo
- Publication number
- ES221370A1 ES221370A1 ES0221370A ES221370A ES221370A1 ES 221370 A1 ES221370 A1 ES 221370A1 ES 0221370 A ES0221370 A ES 0221370A ES 221370 A ES221370 A ES 221370A ES 221370 A1 ES221370 A1 ES 221370A1
- Authority
- ES
- Spain
- Prior art keywords
- phosphorothiolothionate
- atom
- diethyl
- attached
- formula
- 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
- 230000000361 pesticidal effect Effects 0.000 title abstract 3
- 239000002253 acid Substances 0.000 title 1
- -1 alkyl radicals Chemical class 0.000 abstract 8
- 125000004432 carbon atom Chemical group C* 0.000 abstract 8
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 6
- 229910052757 nitrogen Inorganic materials 0.000 abstract 6
- 229910052799 carbon Inorganic materials 0.000 abstract 5
- 235000015097 nutrients Nutrition 0.000 abstract 5
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 abstract 4
- 125000001931 aliphatic group Chemical group 0.000 abstract 4
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 4
- 239000012752 auxiliary agent Substances 0.000 abstract 4
- 125000000623 heterocyclic group Chemical group 0.000 abstract 4
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 3
- 125000004437 phosphorous atom Chemical group 0.000 abstract 3
- 229910052698 phosphorus Inorganic materials 0.000 abstract 3
- 229920006395 saturated elastomer Polymers 0.000 abstract 3
- OZGAJMXOQKGWKB-UHFFFAOYSA-N 1-(dipropylamino)-3-ethylsulfanylpropan-2-ol Chemical compound C(C)SCC(CN(CCC)CCC)O OZGAJMXOQKGWKB-UHFFFAOYSA-N 0.000 abstract 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 abstract 2
- 239000004141 Sodium laurylsulphate Substances 0.000 abstract 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 2
- 229910052783 alkali metal Inorganic materials 0.000 abstract 2
- 239000000440 bentonite Substances 0.000 abstract 2
- 229910000278 bentonite Inorganic materials 0.000 abstract 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 abstract 2
- 239000004202 carbamide Substances 0.000 abstract 2
- 239000000969 carrier Substances 0.000 abstract 2
- PHHWLDOIMGFHOZ-UHFFFAOYSA-L disodium;dinaphthalen-1-ylmethanedisulfonate Chemical compound [Na+].[Na+].C1=CC=C2C(C(C=3C4=CC=CC=C4C=CC=3)(S(=O)(=O)[O-])S([O-])(=O)=O)=CC=CC2=C1 PHHWLDOIMGFHOZ-UHFFFAOYSA-L 0.000 abstract 2
- 239000003292 glue Substances 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 abstract 2
- 235000019341 magnesium sulphate Nutrition 0.000 abstract 2
- 239000003960 organic solvent Substances 0.000 abstract 2
- 230000001931 phytocidal effect Effects 0.000 abstract 2
- 239000011347 resin Substances 0.000 abstract 2
- 229920005989 resin Polymers 0.000 abstract 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- 239000000454 talc Substances 0.000 abstract 2
- 229910052623 talc Inorganic materials 0.000 abstract 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- 210000002268 wool Anatomy 0.000 abstract 2
- IQHIFJVDTZSMEK-UHFFFAOYSA-N 1-chloro-3-ethylsulfanylpropan-2-ol Chemical compound CCSCC(O)CCl IQHIFJVDTZSMEK-UHFFFAOYSA-N 0.000 abstract 1
- JVPSQYCVDARKSD-UHFFFAOYSA-N 2-chloro-3-ethylsulfanyl-N,N-dipropylpropan-1-amine Chemical compound ClC(CN(CCC)CCC)CSCC JVPSQYCVDARKSD-UHFFFAOYSA-N 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003396 thiol group Chemical group [H]S* 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
- C07F9/16—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
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 (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2321254A GB783281A (en) | 1954-08-10 | 1954-08-10 | New pesticidal basic esters of phosphorothiolothionic acid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES221370A1 true ES221370A1 (es) | 1955-11-16 |
Family
ID=10191970
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0221370A Expired ES221370A1 (es) | 1954-08-10 | 1955-04-23 | PROCEDIMIENTO DE FABRICACIoN DE NUEVOS ÉSTERES BáSICOS PESTICIDAS DE áCIDO FOSFOROTIOLOTIoNICO |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE537490A (hu) |
| DE (1) | DE1062254B (hu) |
| ES (1) | ES221370A1 (hu) |
| GB (1) | GB783281A (hu) |
-
0
- BE BE537490D patent/BE537490A/xx unknown
-
1954
- 1954-08-10 GB GB2321254A patent/GB783281A/en not_active Expired
-
1955
- 1955-04-23 ES ES0221370A patent/ES221370A1/es not_active Expired
- 1955-07-28 DE DEI10479A patent/DE1062254B/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| BE537490A (hu) | |
| GB783281A (en) | 1957-09-18 |
| DE1062254B (de) | 1959-07-30 |
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