GB1327905A - Latex stimulation - Google Patents
Latex stimulationInfo
- Publication number
- GB1327905A GB1327905A GB2534772A GB2534772A GB1327905A GB 1327905 A GB1327905 A GB 1327905A GB 2534772 A GB2534772 A GB 2534772A GB 2534772 A GB2534772 A GB 2534772A GB 1327905 A GB1327905 A GB 1327905A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloroethyl
- give
- reacted
- phosphonic
- acid
- 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
- 239000004816 latex Substances 0.000 title 1
- 229920000126 latex Polymers 0.000 title 1
- 230000000638 stimulation Effects 0.000 title 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- LOUZURPQCYZSJH-UHFFFAOYSA-N 1-chloro-2-dichlorophosphorylethane Chemical compound ClCCP(Cl)(Cl)=O LOUZURPQCYZSJH-UHFFFAOYSA-N 0.000 abstract 2
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 abstract 1
- FOWZCIWTKGEIST-UHFFFAOYSA-N 2-chloroethyl-di(propan-2-yloxy)-sulfanylidene-lambda5-phosphane Chemical compound C(C)(C)OP(OC(C)C)(=S)CCCl FOWZCIWTKGEIST-UHFFFAOYSA-N 0.000 abstract 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 abstract 1
- UDBZUFZWXJJBAL-UHFFFAOYSA-N 4-chloro-5-methylpyrimidin-2-amine Chemical compound CC1=CN=C(N)N=C1Cl UDBZUFZWXJJBAL-UHFFFAOYSA-N 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
- -1 Haloethyl phosphonic acid derivatives Chemical class 0.000 abstract 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 abstract 1
- 229940042400 direct acting antivirals phosphonic acid derivative Drugs 0.000 abstract 1
- 150000002978 peroxides Chemical class 0.000 abstract 1
- LLWDULGXUFLRGH-UHFFFAOYSA-N propan-2-yloxy(propan-2-ylsulfanyl)phosphinous acid Chemical compound CC(C)OP(O)SC(C)C LLWDULGXUFLRGH-UHFFFAOYSA-N 0.000 abstract 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-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
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
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)
Abstract
1327905 Haloethyl phosphonic acid derivatives AMCHEM PRODUCTS Inc 30 May 1972 [27 May 1971] 25347/72 Heading C2P [Also in Division C1] Example 1. 2-Bromoethyl phosphonic acid is prepared by reacting ethylene dibromide with triethyl phosphite to give the diethyl ester which is then hydrolysed in hydrobromic acid. Example 2. Diethylamine and 2-chloroethyl phosphonic dichloride are reacted in benzene to give 2-chloroethyl phosphoni-di-(N,N-diethyl)- amide. Example 3. Ammonia is reacted with 2- chloroethyl phosphonic dichloride to give 2- chloroethyl phosphonidiamide. Example 4. Vinyl chloride is reacted with di-isopropyl thiophosphite containing di-tbutyl peroxide to give 2-chloroethyl-thiophosphonic acid di-isopropyl ester.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14766671A | 1971-05-27 | 1971-05-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1327905A true GB1327905A (en) | 1973-08-22 |
Family
ID=22522424
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2534772A Expired GB1327905A (en) | 1971-05-27 | 1972-05-30 | Latex stimulation |
Country Status (2)
| Country | Link |
|---|---|
| GB (1) | GB1327905A (en) |
| MY (1) | MY7400159A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4042370A (en) * | 1974-09-18 | 1977-08-16 | Sandoz Ltd. | Di-(acyloxyalkyl)-β-haloethane-phosphonates and dithiophosphonates and use as plant growth regulators |
-
1972
- 1972-05-30 GB GB2534772A patent/GB1327905A/en not_active Expired
-
1974
- 1974-12-30 MY MY7400159A patent/MY7400159A/en unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4042370A (en) * | 1974-09-18 | 1977-08-16 | Sandoz Ltd. | Di-(acyloxyalkyl)-β-haloethane-phosphonates and dithiophosphonates and use as plant growth regulators |
Also Published As
| Publication number | Publication date |
|---|---|
| MY7400159A (en) | 1974-12-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| 732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
| 732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
| PE20 | Patent expired after termination of 20 years |