CAS 15805-73-9
:Vinyl carbamate
Description:
Vinyl carbamate is an organic compound characterized by its vinyl group (–CH=CH2) and a carbamate functional group (–OC(=O)NR2). It is a colorless to pale yellow liquid with a faint odor, and it is known for its reactivity, particularly in polymerization processes. Vinyl carbamate is soluble in organic solvents and exhibits moderate stability under standard conditions, although it can undergo hydrolysis in the presence of water, leading to the formation of carbamic acid and other byproducts. This compound is primarily used in the synthesis of polymers and copolymers, as well as in the production of various chemical intermediates. Due to its potential reactivity, it is important to handle vinyl carbamate with care, as it may pose health risks upon exposure. Safety measures should be taken to avoid inhalation or skin contact, and it is advisable to work with this substance in a well-ventilated area or under a fume hood. Overall, vinyl carbamate is a versatile compound with applications in materials science and chemical manufacturing.
Formula:C3H5NO2
InChI:InChI=1S/C3H5NO2/c1-2-6-3(4)5/h2H,1H2,(H2,4,5)
InChI key:InChIKey=LVLANIHJQRZTPY-UHFFFAOYSA-N
SMILES:O(C(N)=O)C=C
Synonyms:- Carbamic acid, ethenyl ester
- Carbamic acid, vinyl ester
- Ethenyl Carbamate
- Ethenyl Ester Carbamic Acid
- Nsc 133266
- Vinyl Ester Carbamic Acid
- Vinyl carbamate
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Found 3 products.
Vinyl Carbamate
CAS:Controlled ProductApplications A potent promutagen. Also mutagenic to Salmonella typhimurium TA 1535 and TA 100 in the presence of reduced nicotinamide adenine dinucleotide phosphate-fortified rat or mouse liver mitochondrial supernatant fractions.
References Dahl, G.A., et al.: Cancer Research, 38, 3793 (1978), Dahl, G.A., et al.: Cancer Research, 40, 1194 (1980), Leithauser, M.T. et al.: Carcinogenesis, 11, 3, 463 (1990)Formula:C3H5NO2Color and Shape:NeatMolecular weight:87.08Vinyl carbamate
CAS:Vinyl carbamate is a reactive chemical that is carcinogenic in animals. It can be synthesized by reacting vinyl chloride with anhydrous ammonia at high temperature and pressure. Vinyl carbamate is used in the synthesis of polymers, such as epidermal growth factor and hydroxyl group-containing proteins. It also has been used to prepare monoclonal antibodies against the cd-1 mouse lymphoma cell line. However, it should not be used at low doses due to its carcinogenic potential. The carcinogenic effects of vinyl carbamate have been observed in mice after administration of a single dose (2 mg/kg) or repeated doses (0.3 mg/kg per day for 5 days).Formula:C3H5NO2Purity:Min. 95%Color and Shape:White To Off-White SolidMolecular weight:87.08 g/mol


