Ethyl 3-acetoxyacrylate

Base Information

Chemical Name:Ethyl 3-acetoxyacrylate
CAS No.:61381-00-8
Molecular Formula:C7H10 O4
Molecular Weight:158.154
Hs Code.:2918990090
European Community (EC) Number:262-751-2
Nikkaji Number:J1.100.013D,J279.619H
Mol file:61381-00-8.mol

Synonyms:acetoxyacrylic acid ethyl ester;ethyl acetoxyacrylate

Suppliers and Price of Ethyl 3-acetoxyacrylate

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

Total 5 raw suppliers

Chemical Property of Ethyl 3-acetoxyacrylate

Chemical Property:

Vapor Pressure:0.406mmHg at 25°C
Boiling Point:196.1°C at 760 mmHg
Flash Point:89.7°C
PSA：52.60000
Density:1.093g/cm³
LogP:0.62630
XLogP3:0.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:158.05790880
Heavy Atom Count:11
Complexity:171

Purity/Quality:: 98%Min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C=COC(=O)C
Isomeric SMILES:CCOC(=O)/C=C/OC(=O)C

Technology Process of Ethyl 3-acetoxyacrylate

There total 5 articles about Ethyl 3-acetoxyacrylate 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: 46.0%

: 1-(3'-ethoxycarbonylethenyl)-3-methylimidazolium bromide

: 3375-31-3
palladium diacetate

: 61381-00-8
ethyl (E/Z)-3-acetyloxy-2-propenoate

: trans-dibromo[3-methylimidazol][(1-(3'-ethoxycarbonylethenyl)-3-methylimidazolin-2-yliden)]palladium(II)

Guidance literature:: In dimethyl sulfoxide; (Ar), Schlenk techniques; Pd(CH3CO2)2 and ylidene ligand dissolved in DMSO, stirred for 3 h at 50°C, heated to 90°C for 1 h; solvent removed under vac., residue stirred with THF, filtered, solvent evapd. under vac., recrystd. from THF; elem. anal.;
DOI:10.1016/j.molstruc.2008.05.037