ES247459A1 - Un método para obtener una preparacion para combatir mohos - Google Patents
Un método para obtener una preparacion para combatir mohosInfo
- Publication number
- ES247459A1 ES247459A1 ES0247459A ES247459A ES247459A1 ES 247459 A1 ES247459 A1 ES 247459A1 ES 0247459 A ES0247459 A ES 0247459A ES 247459 A ES247459 A ES 247459A ES 247459 A1 ES247459 A1 ES 247459A1
- Authority
- ES
- Spain
- Prior art keywords
- compound
- chloro
- sulphur atom
- dimethylamido
- bis
- 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
- 150000003013 phosphoric acid derivatives Chemical class 0.000 title 1
- SGYDKALSBFBIFE-UHFFFAOYSA-N tris(2,3,4,5,6-pentachlorophenyl) phosphate Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1OP(=O)(OC=1C(=C(Cl)C(Cl)=C(Cl)C=1Cl)Cl)OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl SGYDKALSBFBIFE-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 239000002904 solvent Substances 0.000 abstract 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 abstract 3
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 abstract 3
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 abstract 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 2
- 239000004480 active ingredient Substances 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 239000007795 chemical reaction product Substances 0.000 abstract 2
- 239000000428 dust Substances 0.000 abstract 2
- 230000000749 insecticidal effect Effects 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 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
- 239000007787 solid Substances 0.000 abstract 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- LLMLGZUZTFMXSA-UHFFFAOYSA-N 2,3,4,5,6-pentachlorobenzenethiol Chemical compound SC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LLMLGZUZTFMXSA-UHFFFAOYSA-N 0.000 abstract 1
- 235000013162 Cocos nucifera Nutrition 0.000 abstract 1
- 244000060011 Cocos nucifera Species 0.000 abstract 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 abstract 1
- 241000196324 Embryophyta Species 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
- 239000005909 Kieselgur Substances 0.000 abstract 1
- 241000208125 Nicotiana Species 0.000 abstract 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 229920001131 Pulp (paper) Polymers 0.000 abstract 1
- 239000013543 active substance Substances 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 229960000892 attapulgite Drugs 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- 239000012876 carrier material Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000004927 clay Substances 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 abstract 1
- 229910000514 dolomite Inorganic materials 0.000 abstract 1
- 239000010459 dolomite Substances 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 239000012530 fluid Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229910052625 palygorskite Inorganic materials 0.000 abstract 1
- 239000003209 petroleum derivative Substances 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 abstract 1
- 229940031826 phenolate Drugs 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical class OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 abstract 1
- 235000011118 potassium hydroxide Nutrition 0.000 abstract 1
- 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 235000011121 sodium hydroxide Nutrition 0.000 abstract 1
- -1 solvent naphtha Chemical compound 0.000 abstract 1
- 239000002641 tar oil Substances 0.000 abstract 1
- 239000004563 wettable powder Substances 0.000 abstract 1
- 239000008096 xylene 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
- C07F9/22—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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL225241 | 1958-02-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES247459A1 true ES247459A1 (es) | 1959-10-16 |
Family
ID=19751136
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0247459A Expired ES247459A1 (es) | 1958-02-24 | 1959-02-21 | Un método para obtener una preparacion para combatir mohos |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3038924A (es) |
| BE (1) | BE576063A (es) |
| CH (1) | CH379193A (es) |
| DE (1) | DE1201116B (es) |
| ES (1) | ES247459A1 (es) |
| FR (1) | FR1247334A (es) |
| GB (1) | GB920117A (es) |
| NL (2) | NL225241A (es) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3157568A (en) * | 1959-02-16 | 1964-11-17 | Philips Corp | Bis(dimethylamido)pentachlorophenyl fungicidal compositions |
| NL128817C (es) * | 1959-04-16 | |||
| US3089808A (en) * | 1959-08-06 | 1963-05-14 | Philips Corp | Acaricidal diamido phosphate phenol complex |
| US3351682A (en) * | 1959-12-18 | 1967-11-07 | Monsanto Co | Omicron-aryl dialkylphosphinothioates |
| DE1196897B (de) * | 1962-08-23 | 1965-07-15 | Bayer Ag | Rodentizide Mittel |
| US3346668A (en) * | 1964-04-30 | 1967-10-10 | Monsanto Res Corp | Fluorine-containing phosphinates |
| US3340331A (en) * | 1964-04-30 | 1967-09-05 | Monsanto Res Corp | Fluorine-containing phosphinates |
| US3397270A (en) * | 1967-01-25 | 1968-08-13 | Monsanto Co | Method for controlling and eradicating insects with phosphoroamidate sterilants |
| US3923733A (en) * | 1973-04-13 | 1975-12-02 | American Cyanamid Co | Polyolefin light stabilizers |
| US3984348A (en) * | 1973-11-05 | 1976-10-05 | American Cyanamid Company | Polyolefin light stabilizers |
| US3956486A (en) * | 1974-12-30 | 1976-05-11 | Stauffer Chemical Company | Insecticidal phthalimidothiophosphates activated with certain phosphorothionates |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH246915A (de) * | 1944-06-13 | 1947-02-15 | Ag J R Geigy | Schädlingsbekämpfungsmittel. |
| US2642406A (en) * | 1948-04-06 | 1953-06-16 | Eastman Kodak Co | Solutions of polymers of acrylonitrile |
| US2615037A (en) * | 1948-10-15 | 1952-10-21 | Dow Chemical Co | O,o-di(4-chlorophenyl) n-alkylamidothiophosphates |
| US2552538A (en) * | 1948-10-15 | 1951-05-15 | Dow Chemical Co | Diamidothiophosphates |
| US2615038A (en) * | 1948-10-15 | 1952-10-21 | Dow Chemical Co | O,o-di(polyhalophenyl) n-substituted amidothiophosphates |
| NL79191C (es) * | 1949-02-02 | |||
| US2611729A (en) * | 1949-11-01 | 1952-09-23 | Standard Oil Dev Co | Insecticidal compositions containing hydrocarbon esters of diethyl dithiophosphoric acid |
| US2818406A (en) * | 1954-04-26 | 1957-12-31 | Phillips Petroleum Co | Phosphonic diamides |
| DE1067016B (de) * | 1954-12-04 | 1959-10-15 | Farbenfabriken Bayer Aktiengesellschaft Leverkusen-Bayerwerk | Verfahren zur Her stellung von organischen Phosphorver bmdungen |
| US2855426A (en) * | 1956-04-04 | 1958-10-07 | Dow Chemical Co | O-(cyclohexylphenyl) phosphoroamidothioates |
| US2832745A (en) * | 1956-08-31 | 1958-04-29 | Shea Chemical Corp | Aqueous flameproofing compositions and cellulosic materials treated therewith |
-
0
- NL NL100594D patent/NL100594C/xx active
- NL NL225241D patent/NL225241A/xx unknown
- BE BE576063D patent/BE576063A/xx unknown
-
1959
- 1959-02-16 US US793294A patent/US3038924A/en not_active Expired - Lifetime
- 1959-02-20 GB GB5924/59A patent/GB920117A/en not_active Expired
- 1959-02-21 ES ES0247459A patent/ES247459A1/es not_active Expired
- 1959-02-21 DE DEN16305A patent/DE1201116B/de active Pending
- 1959-02-21 CH CH6987959A patent/CH379193A/de unknown
- 1959-02-23 FR FR787472A patent/FR1247334A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NL225241A (es) | |
| US3038924A (en) | 1962-06-12 |
| GB920117A (en) | 1963-03-06 |
| NL100594C (es) | |
| FR1247334A (fr) | 1960-12-02 |
| DE1201116B (de) | 1965-09-16 |
| BE576063A (es) | |
| CH379193A (de) | 1964-06-30 |
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