GB326137A - Process for the manufacture of new organic phosphorus compounds - Google Patents
Process for the manufacture of new organic phosphorus compoundsInfo
- Publication number
- GB326137A GB326137A GB3535728A GB3535728A GB326137A GB 326137 A GB326137 A GB 326137A GB 3535728 A GB3535728 A GB 3535728A GB 3535728 A GB3535728 A GB 3535728A GB 326137 A GB326137 A GB 326137A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cresol
- oxide
- phosphorus compounds
- organic phosphorus
- hydroxy
- 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
- 150000002903 organophosphorus compounds Chemical class 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 3
- 239000007859 condensation product Substances 0.000 abstract 2
- -1 o- and pchloraphenol Chemical compound 0.000 abstract 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 abstract 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 2
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 abstract 2
- SMFHPCZZAAMJJO-UHFFFAOYSA-N 2-chloro-5-methylphenol Chemical compound CC1=CC=C(Cl)C(O)=C1 SMFHPCZZAAMJJO-UHFFFAOYSA-N 0.000 abstract 1
- YPNZJHFXFVLXSE-UHFFFAOYSA-N 2-chloro-6-methylphenol Chemical compound CC1=CC=CC(Cl)=C1O YPNZJHFXFVLXSE-UHFFFAOYSA-N 0.000 abstract 1
- IJALWSVNUBBQRA-UHFFFAOYSA-N 4-Isopropyl-3-methylphenol Chemical compound CC(C)C1=CC=C(O)C=C1C IJALWSVNUBBQRA-UHFFFAOYSA-N 0.000 abstract 1
- SCWBSTVOWDDYHH-UHFFFAOYSA-N 4-amino-2,6-dichlorophenol;4-aminophenol Chemical compound NC1=CC=C(O)C=C1.NC1=CC(Cl)=C(O)C(Cl)=C1 SCWBSTVOWDDYHH-UHFFFAOYSA-N 0.000 abstract 1
- HJSPWKGEPDZNLK-UHFFFAOYSA-N 4-benzylphenol Chemical compound C1=CC(O)=CC=C1CC1=CC=CC=C1 HJSPWKGEPDZNLK-UHFFFAOYSA-N 0.000 abstract 1
- ROGAWZUXVDNJFF-UHFFFAOYSA-N 4-chloro-2-(2-methylpropyl)phenol Chemical compound CC(C)CC1=CC(Cl)=CC=C1O ROGAWZUXVDNJFF-UHFFFAOYSA-N 0.000 abstract 1
- KFZXVMNBUMVKLN-UHFFFAOYSA-N 4-chloro-5-methyl-2-propan-2-ylphenol Chemical compound CC(C)C1=CC(Cl)=C(C)C=C1O KFZXVMNBUMVKLN-UHFFFAOYSA-N 0.000 abstract 1
- CYYZDBDROVLTJU-UHFFFAOYSA-N 4-n-Butylphenol Chemical compound CCCCC1=CC=C(O)C=C1 CYYZDBDROVLTJU-UHFFFAOYSA-N 0.000 abstract 1
- BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
- 241000238631 Hexapoda Species 0.000 abstract 1
- 239000005844 Thymol Substances 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000004494 ethyl ester group Chemical group 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 244000005700 microbiome Species 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 abstract 1
- 229960000790 thymol Drugs 0.000 abstract 1
- FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/535—Organo-phosphoranes
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)
Abstract
326,137. Carpmael, A., (I. G. Farbenindustrie Akt.-Ges.). Nov. 30, 1928. Proofing against vermin; proofing-compositions. -Organic phosphorus compounds, prepared by condensing a triarylphosphine oxide with a compound containing a phenolic hydroxy group, are useful for the protection of materials against micro-organisms and insects such as moth caterpillars. The following organic phosphorus compounds are referred to:-(1) condensation product of o-tritolylphosphine oxide with phenol, (2) condensation products of triphenylphosphine oxide with phenol, om- and p-cresol, o- and pchloraphenol, 4-benzylphenol, thymol, 1-methyl- 3-hydroxy-4-isopropyl-6-chlorobenzene, 2: 6-dichlorophenol, 2: 4: 6-trichlorophenol, symxylenol, 6-chloro-2-cresol. 6-chloro-3-cresol, phydroxybenzoic acid ethyl ester, p-nitrophenol, pyrocatechin monoethyl ether, resorcinol, phydroxybenzaldehyde, alpha- and #-naphthol, mhydroxydiethylaniline, ar-tetrahydro-#-naphthol, 4-n-butylphenol, 2:4-dichlorophenol, 2-isobutyl- 4-chlorophenol, 1-methyl-3-hydroxy-6-isopropylbenzene and 1-hydroxyphenyl-3: 4-dicarboxylic acid dibutyl ester. The Provisional Specification states that any phosphine oxide may be employed.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3535728A GB326137A (en) | 1928-11-30 | 1928-11-30 | Process for the manufacture of new organic phosphorus compounds |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3535728A GB326137A (en) | 1928-11-30 | 1928-11-30 | Process for the manufacture of new organic phosphorus compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB326137A true GB326137A (en) | 1930-02-28 |
Family
ID=10376831
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3535728A Expired GB326137A (en) | 1928-11-30 | 1928-11-30 | Process for the manufacture of new organic phosphorus compounds |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB326137A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2599512A (en) * | 1950-04-21 | 1952-06-03 | Dow Chemical Co | O-2, 4, 6-trichlorophenyl o, o-dialkylthiophosphates |
| US2599516A (en) * | 1950-03-30 | 1952-06-03 | Dow Chemical Co | O-2, 4, 5-trichlorophenyl o, o-dialkylthiophosphates |
| US2599515A (en) * | 1950-03-30 | 1952-06-03 | Dow Chemical Co | O-2, 4, 5-trichlorophenyl o, o-dialkylphosphates |
| US2599375A (en) * | 1950-04-21 | 1952-06-03 | Lewis R Drake | 2,4,6-trichlorophenyl dialkylphosphates |
| US2754242A (en) * | 1953-03-11 | 1956-07-10 | Monsanto Chemicals | Process of combatting insects utilizing phosphinates |
-
1928
- 1928-11-30 GB GB3535728A patent/GB326137A/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2599516A (en) * | 1950-03-30 | 1952-06-03 | Dow Chemical Co | O-2, 4, 5-trichlorophenyl o, o-dialkylthiophosphates |
| US2599515A (en) * | 1950-03-30 | 1952-06-03 | Dow Chemical Co | O-2, 4, 5-trichlorophenyl o, o-dialkylphosphates |
| US2599512A (en) * | 1950-04-21 | 1952-06-03 | Dow Chemical Co | O-2, 4, 6-trichlorophenyl o, o-dialkylthiophosphates |
| US2599375A (en) * | 1950-04-21 | 1952-06-03 | Lewis R Drake | 2,4,6-trichlorophenyl dialkylphosphates |
| US2754242A (en) * | 1953-03-11 | 1956-07-10 | Monsanto Chemicals | Process of combatting insects utilizing phosphinates |
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