Triethyl 2,2-dichloro-2-phosphonoacetate

Base Information

Chemical Name:Triethyl 2,2-dichloro-2-phosphonoacetate
CAS No.:5823-12-1
Molecular Formula:C8H15Cl2O5P
Molecular Weight:293.084
Hs Code.:
European Community (EC) Number:621-801-7
DSSTox Substance ID:DTXSID60393920
Nikkaji Number:J1.156.735E
Wikidata:Q82192978
Mol file:5823-12-1.mol

Synonyms:Triethyl 2,2-dichloro-2-phosphonoacetate;5823-12-1;ethyl 2,2-dichloro-2-diethoxyphosphorylacetate;ETHYL 2,2-DICHLORO-2-(DIETHOXYPHOSPHORYL)ACETATE;Forstenon;SBB057702;SCHEMBL18956879;DTXSID60393920;MFCD00192517;AKOS017343311;Diethyl dichloro(ethoxycarbonyl)methylphosphonate;Triethyl 2,2-dichloro-2-phosphonoacetate, 98%;Dichloro-(diethoxy-phosphoryl)-acetic acid ethyl ester

Suppliers and Price of Triethyl 2,2-dichloro-2-phosphonoacetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Sigma-Aldrich
Triethyl 2,2-dichloro-2-phosphonoacetate 98%
5ml
$ 27.80

American Custom Chemicals Corporation
TRIETHYL 2,2-DICHLORO-2-PHOSPHONOACETATE 95.00%
5ML
$ 777.89

Total 6 raw suppliers

Chemical Property of Triethyl 2,2-dichloro-2-phosphonoacetate

Chemical Property:

Vapor Pressure:0.000513mmHg at 25°C
Refractive Index:n20/D 1.456(lit.)
Boiling Point:84-86 °C0.01 mm Hg(lit.)
Flash Point:>230 °F
PSA：71.64000
Density:1.289 g/mL at 25 °C(lit.)
LogP:2.94700
XLogP3:1.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:292.0034160
Heavy Atom Count:16
Complexity:272

Purity/Quality:

95% ^*data from raw suppliers

Triethyl 2,2-dichloro-2-phosphonoacetate 98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26-36

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C(P(=O)(OCC)OCC)(Cl)Cl
Uses Ethyl 2,2-Dichloro-2-diethoxyphosphorylacetate acts as a reagent in the synthesis of halogenated phosphonoacetate esters. It is also used as a reagent for cotton insecticides preparations.

Technology Process of Triethyl 2,2-dichloro-2-phosphonoacetate

There total 2 articles about Triethyl 2,2-dichloro-2-phosphonoacetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%

: 867-13-0
diethoxyphosphoryl-acetic acid ethyl ester

: 5823-12-1
ethyl 2,2-dichloro-2-diethoxyphosphorylacetate

Guidance literature:: With sodium hypochlorite; for 0.0833333h;
DOI:10.1021/jo00376a092

Reference yield:

: 5823-12-1
ethyl 2,2-dichloro-2-diethoxyphosphorylacetate

Guidance literature:: Ethoxycarbonylmethyl-phosphonsaeure-diethylester, Cl2;

Reference yield: 45.0%

: 5823-12-1
ethyl 2,2-dichloro-2-diethoxyphosphorylacetate

: 7071-12-7
triethyl 2-chloro-2-phosphonoacetate

: methoxyphenyl-3 chloro-2 propenoate d'ethyle

Guidance literature:: With tetramethylammonium tetrafluoroborate; 4-methoxy-benzaldehyde; In N,N-dimethyl-formamide; Ambient temperature; controlled potential electrolysis; cathode: Hg; electrode ref.: AgI/Ag;