CAS 598-16-3

1,1,2-Tribromoethene

Description:

1,1,2-Tribromoethene, with the CAS number 598-16-3, is a halogenated organic compound characterized by the presence of three bromine atoms attached to a two-carbon ethene backbone. This compound is a colorless liquid at room temperature and is known for its distinctive sweet odor. It is classified as a volatile organic compound (VOC) and is insoluble in water but soluble in organic solvents. The presence of multiple bromine atoms contributes to its reactivity, making it a potential intermediate in various chemical reactions, particularly in organic synthesis. 1,1,2-Tribromoethene is also of interest in environmental chemistry due to its potential role as a pollutant and its implications in studies related to brominated flame retardants. Safety considerations are important when handling this compound, as it may pose health risks through inhalation or skin contact. Proper storage and disposal methods are essential to mitigate environmental impact and ensure safety in laboratory settings.

Formula: C₂HBr₃

InChI: InChI=1S/C2HBr3/c3-1-2(4)5/h1H

InChI key: InChIKey=OZVJKTHTULCNHB-UHFFFAOYSA-N

SMILES: C(=CBr)(Br)Br

Synonyms:

• 1,1,2-Tribromoethene
• 1,1,2-Tribromoethylene
• Brn 1736791
• Ethene, 1,1,2-tribromo-
• Ethene, tribromo-
• Ethylene tribromide
• Ethylene, tribromo-
• Ethylene, tribromo- (VAN) (8CI)
• Nsc 343621
• Tribromoethene
• 4-01-00-00722 (Beilstein Handbook Reference)

Tribromoethylene

CAS: 598-16-3

Formula: C₂HBr₃

Purity: >97.0%(GC)

Color and Shape: Colorless to Light yellow to Light orange clear liquid

Molecular weight: 264.74

Ref: 3B-T0794

Tribromoethylene

CAS: 598-16-3

Purity: 97.0%

Color and Shape: Liquid, Clear

Molecular weight: 264.74200439453125

Ref: 10-F172800

Tribromoethylene

CAS: 598-16-3

Tribromoethylene is a reactive, hydroxyl-containing compound that has been used as a cross-linking agent in the production of polymers. It is a colorless liquid with an unpleasant odor. Tribromoethylene has many uses including as an antioxidant and a stabilizer for rubber, plastics, and paints. In addition to its use as a reactive functional group, tribromoethylene also has long-term toxicity in CD-1 mice. This toxicity may be due to the ability of tribromoethylene to produce epoxides through oxidation by hydrogen fluoride or other peroxides. Epoxides are known to disrupt cellular energy metabolism and cause cell death by reacting with lysine residues on proteins. The mechanism for this toxicity is not well understood but may involve cross-linking of proteins and DNA.

Formula: C₂HBr₃

Purity: Min. 95%

Molecular weight: 264.74 g/mol

Ref: 3D-AAA59816