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About This Item
Linear Formula:
ClCH2COOCH=CH2
CAS Number:
Molecular Weight:
120.53
Beilstein:
1745172
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
≥99.0%
contains
~0.01% hydroquinone monomethyl ether as stabilizer
refractive index
n20/D 1.444
density
1.192 g/mL at 20 °C
storage temp.
2-8°C
SMILES string
ClCC(=O)OC=C
InChI
1S/C4H5ClO2/c1-2-7-4(6)3-5/h2H,1,3H2
InChI key
XJELOQYISYPGDX-UHFFFAOYSA-N
Related Categories
Application
Vinyl chloroacetate was used to study the effect of the electron-withdrawing groups on the ligand in a series of bis(acetylacetonate)cobalt(II) derivatives.
Other Notes
Used for the enzyme-catalyzed, regioselective acylation of carbohydrates
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Certificates of Analysis (COA)
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E.W. Holla
Angewandte Chemie (International Edition in English), 101, 222-222 (1989)
Radical (co) polymerization of vinyl chloroacetate and N-vinylpyrrolidone mediated by bis (acetylacetonate) cobalt derivatives.
Kaneyoshi H and Matyjaszewski K.
Macromolecules, 39(8), 2757-2763 (2006)
Jérémie Brand et al.
Carbohydrate polymers, 169, 189-197 (2017-05-16)
Herein we propose a versatile method for the surface tailoring of cellulose nanocrystals (CNCs) based on the reactivity of vinyl ester molecules toward the accessible hydroxyl groups located at the surface of the nanoparticles. CNCs produced from wood pulp were
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