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About This Item
Linear Formula:
ClCH2COOCH=CH2
CAS Number:
Molecular Weight:
120.53
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-834-3
Beilstein/REAXYS Number:
1745172
MDL number:
Assay:
≥99.0%
Product Name
Vinyl chloroacetate, ≥99.0%
InChI key
XJELOQYISYPGDX-UHFFFAOYSA-N
InChI
1S/C4H5ClO2/c1-2-7-4(6)3-5/h2H,1,3H2
SMILES string
ClCC(=O)OC=C
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
functional group
chloro
ester
storage temp.
2-8°C
Quality Level
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
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
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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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