Cat. No JK124234_100_G
J&K Chemical

Product Information

Product Name
β-Bromostyrene, 97%
Brand Name
J&K
Product Number
124234
CAS
103-64-0
Molecular Formula
C8H7Br
Molecular Weight
183.05
SDS Document
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
(Z)-β-bromostyrene
PubChem CID
7667
IUPAC Name
2-bromoethenylbenzene
InChI Key
YMOONIIMQBGTDU-UHFFFAOYSA-N
SMILES
C1=CC=C(C=C1)C=CBr

Properties

Density
1.427
Melting Point
7
Boiling Point
220.9
Flash Point
101.7
n20D
1.608

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H302
Precautionary Statement
P264
P270
P330
Storage Condition
Store at 2-8℃

References Data Source From Pubchem

Polymer Supported Ruthenium and Palladium Based Bi-Metallic Catalyst for Tandem Cross-Coupling/Transfer Hydrogenation

Publication Name: Catalysis Letters
Publication Date: 2026-02-17
DOI: 10.1007/s10562-025-05297-x

Author Correction: Regio- and stereoselective synthesis of tetra- and triarylethenes by N-methylimidodiacetyl boron-directed palladium-catalysed three-component coupling

Publication Name: Communications Chemistry
Publication Date: 2019-03-22
DOI: 10.1038/s42004-019-0137-0|10.1038/s42004-019-0152-1

Synthesis of Alkenyl Nitriles by the Palladium-Catalysed Cyanation of Vinyl Halides with Acetone Cyanohydrin

Publication Name: Synthetic and Biophysical Studies on the Tridachiahydropyrone Family of Natural Products
Publication Date: 2015-08-13
DOI: 10.1007/978-3-319-22069-7_7

Copper(I) Hydroxyapatite Catalyzed Sonogashira Reaction of Alkynes with Styrenyl Bromides. Reaction of cis-Styrenyl Bromides Forming Unsymmetric Diynes

Publication Name: The Journal of Organic Chemistry
Publication Date: 2012-10-08
DOI: 10.1021/jo3015819

Synthesis of Alkenyl Sulfides Through the Iron-Catalyzed Cross-Coupling Reaction of Vinyl Halides with Thiols

Publication Name: The Journal of Organic Chemistry
Publication Date: 2012-06-28
DOI: 10.1021/jo3008397

β-Bromostyrene, 97%

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