ChemicalBook Product Catalog Chemical Reagents Organic reagents Olefin (cyclic and acyclic) 2-Bromostyrene

2-Bromostyrene

2-Bromostyrene Basic information
Product Name:2-Bromostyrene
Synonyms:1-Bromo-2-vinylbenzene, 1-Bromo-2-ethenylbenzene;2-bromoethenylbenzene;benzene,1-bromo-2-ethenyl-;o-Bromovinylbenzene;Styrene, o-bromo-;2-Bromostyrene contains 0.1% 3,5-di-tert-butylcatechol as inhibitor, 97%;2-Bromostyrene, stab. with ca 0.05% 4-tert-butylcatechol;2-Bromostyrene, 97%, stabilized
CAS:2039-88-5
MF:C8H7Br
MW:183.05
EINECS:218-027-3
Product Categories:Monomers;Polymer Science;Styrene and Functionalized Styrene Monomers;Styrenes
Mol File:2039-88-5.mol
2-Bromostyrene Structure
2-Bromostyrene Chemical Properties
Melting point 7°C
Boiling point 102-104 °C/22 mmHg (lit.)
density 1.46 g/mL at 25 °C (lit.)
refractive index n20/D 1.592(lit.)
Fp 186 °F
storage temp. 2-8°C
solubility Miscible with methanol.
form clear liquid
Specific Gravity1.4160
color Colorless to Yellow
BRN 2323537
InChIKeySSZOCHFYWWVSAI-UHFFFAOYSA-N
CAS DataBase Reference2039-88-5(CAS DataBase Reference)
NIST Chemistry ReferenceBenzene, 1-bromo-2-ethenyl-(2039-88-5)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HazardClass IRRITANT
HS Code 29036990
MSDS Information
ProviderLanguage
1-Bromo-2-vinylbenzene English
SigmaAldrich English
ALFA English
2-Bromostyrene Usage And Synthesis
Chemical PropertiesClear colorless liquid
Uses2-Bromostyrene is used as a cross linking agent in fire-resistant bromostyrene-crosslinked polyesters. Further, it is used to prepare trans-1-(2-bromophenyl)-2-(3-bromophenyl)ethene by reacting with 1-bromo-3-iodo-benzene, involving palladium(II) acetate as catalyst.
2-Bromostyrene Preparation Products And Raw materials
Preparation Products2,3-dimethyl-1H-indene-->Benzoic acid, 2-ethenyl- (9CI)-->2-Hydroxystyrene-->2-AMINOSTYRENE-->1-(2-Bromo-phenyl)-2-(1,3-dioxolan-2-yl)-ethanone-->Diphenylphosphinostyrene
2-BROMO-4-FLUOROCINNAMIC ACID AKOS AU36-M430 METHYL2-CYANO-3-(2-BROMOPHENYL)-ACRYLATE AKOS AU36-M434 Sulfobromophthalein sodium (5E)-5-[(6-BROMO-1,3-BENZODIOXOL-5-YL)METHYLENE]-2-THIOXO-3-[3-(TRIFLUOROMETHYL)PHENYL]-1,3-THIAZOLIDIN-4-ONE 1-(6-BROMO-3,4-METHYLENEDIOXYPHENYL)-2-NITROETHENE TRANS-2-BROMO-BETA-NITROSTYRENE 95 5-[(2-BROMO-4,5-DIMETHOXYPHENYL)METHYLENE]-3-ETHYL-2-THIOXO-1,3-THIAZOLAN-4-ONE (5E)-5-[(6-BROMO-1,3-BENZODIOXOL-5-YL)METHYLENE]-3-(4-METHOXYPHENYL)-2-THIOXO-1,3-THIAZOLIDIN-4-ONE 2-BROMO-4,5-DIMETHOXYCINNAMIC ACID 2-Bromocinnamic acid BROMOSULFALEIN 1-(2-BROMOPHENYL)-2-[1-(4-CHLOROBENZYL)-1H-IMIDAZOL-2-YL]VINYL 2-BROMOBENZOATE AKOS AU36-M431 2-BROMO-5-FLUOROCINNAMIC ACID 3-(2-BROMOPHENYL)-1-(2-HYDROXY-4-METHOXYPHENYL)PROP-2-EN-1-ONE (5E)-5-[(6-BROMO-1,3-BENZODIOXOL-5-YL)METHYLENE]-3-ETHYL-2-THIOXO-1,3-THIAZOLIDIN-4-ONE
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