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15805-73-9

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15805-73-9 Usage

Chemical Properties

White Solid

Uses

Different sources of media describe the Uses of 15805-73-9 differently. You can refer to the following data:
1. 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
2. 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.

General Description

White crystalline solid.

Air & Water Reactions

Moderately water soluble.

Reactivity Profile

Vinyl Carbamate is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates. Vinyl Carbamate is incompatible with strong oxidizing agents, strong acids and strong bases. .

Health Hazard

ACUTE/CHRONIC HAZARDS: When heated to decomposition Vinyl Carbamate emits toxic fumes of carbon monoxide, carbon dioxide and oxides of nitrogen.

Fire Hazard

Flash point data for Vinyl Carbamate are not available; however, Vinyl Carbamate is probably combustible.

Safety Profile

Poison by intraperitoneal route. Questionable carcinogen with experimental neoplastigenic data. Human mutation data reported. When heated to decomposition it emits toxic fumes of NOx. See also ESTERS and CARBAMATES.

Check Digit Verification of cas no

The CAS Registry Mumber 15805-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,0 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15805-73:
(7*1)+(6*5)+(5*8)+(4*0)+(3*5)+(2*7)+(1*3)=109
109 % 10 = 9
So 15805-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H5NO2/c1-2-6-3(4)5/h2H,1H2,(H2,4,5)

15805-73-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name vinyl carbamate

1.2 Other means of identification

Product number -
Other names Carbamic acid,ethenyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15805-73-9 SDS

15805-73-9Related news

Synthesis and properties of Vinyl Carbamate (cas 15805-73-9) epoxide, a possible ultimate electrophilic and carcinogenic metabolite of Vinyl Carbamate (cas 15805-73-9) and ethyl carbamate09/27/2019

Vinyl carbamate reacted with dimethyldioxirane in dry acetone to give a high yield of pure crystalline vinyl carbamate epoxide. This epoxide was characterized by its NMR and MS spectra and elementary analysis. It is unstable at room temperature and has a half-life in water solution of approximat...detailed

15805-73-9Relevant articles and documents

Lysosomal Reacidification Ameliorates Vinyl Carbamate-Induced Toxicity and Disruption on Lysosomal pH

Chen, Wei,Cui, Sunliang,Hu, Dongwen,Li, Yuting,Qi, Jifeng

, p. 8951 - 8961 (2020/09/16)

Ethyl carbamate (EC) is a carcinogen toxicant, commonly found in fermented foods and beverages. The carcinogenic and toxic possibility of EC is thought to be related to its metabolite vinyl carbamate (VC). However, we found interesting mechanisms underlying VC-induced toxicity in this study, which were greatly different from EC. We first conducted a simple synthesis procedure for VC and found that VC possessed higher toxicity but failed to regulate levels of reactive oxygen species, glutathione, and autophagy. Notably, VC treatment resulted in upregulation of lysosomal pH, which was responsible for its cytotoxicity. Cyclic adenosine monophosphate (cAMP) pretreatment could enhance restoration of lysosomal acidity and ameliorate VC-induced damage. Inhibition of protein kinase A and cystic fibrosis transmembrane conductance regulator can block cAMP-induced cytoprotection. Together, our results provided the evidence for novel mechanisms of toxicity and possible protection method under VC exposure, which might give new perspectives on the study of EC-induced toxicity.

Hepatitis C inhibitor tri-peptides

-

, (2008/06/13)

Disclosed herein are compounds of formula (1): wherein Ris hydroxy or NHSO2Rwherein Ris (C1-8)alkyl, (C3-7)cycloalkyl or {(C1-6)alkyl-(C3-7)cycloalkyl}, which are all optionally substituted from 1 to 3 times with halo, cyano, nitro, O-(C1-6)alkyl, amido, amino or phenyl, or Ris C6 or C10 aryl which is optionally substituted from 1 to 3 times with halo, cyano, nitro, (C1-6)alkyl, O-(C1-6) alkyl, amido, amino or phenyl; Ris (C4-6)cycloalkyl; Ris t-btuyl or (C5-6) cycloalkyl and Ris (C4-6)cycloalkyl; or a pharmaceutically acceptable salt thereof. The compounds are useful as inhibitors of HCV NS3 protease.

Vinyl chloroformates and preparation

-

, (2008/06/13)

Vinyl chloroformates are described of formula STR1 in which: R1 =R2 =Cl, Br or a saturated 1-4 carbon atom alkyl or together they form a cycloaliphatic ring of 4-8 carbon atoms; R3 =H when R1 or R2 =a

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