3,3-Dimethylallyl bromide

3,3-Dimethylallyl bromide
  • CAS No.:870-63-3
Other grades of this product :
3,3-Dimethylallyl bromide Basic information
Product Name:3,3-Dimethylallyl bromide
Synonyms:PRENYL BROMIDE;1-Brom-3-methyl-2-buten(4-2,2);1-bromo-3-methyl-2-buten;2-Butene,1-bromo-3-methyl-;3,3-Dimethallylbromide;3-Methyl-1-bromo-2-butene;3-Methyl-2-butyenyl bromide;3-Methyl-butenyl bromide
CAS:870-63-3
MF:C5H9Br
MW:149.03
EINECS:212-799-5
Product Categories:Acyclic;Alkenes;Building Blocks;Chemical Synthesis;Organic Building Blocks
Mol File:870-63-3.mol
3,3-Dimethylallyl bromide Chemical Properties
Melting point -106.7°C (estimate)
Boiling point 82-83 °C150 mm Hg(lit.)
density 1.29 g/mL at 20 °C(lit.)
refractive index n20/D 1.489(lit.)
Fp 88 °F
storage temp. 2-8°C
form Liquid
color Clear colorless, yellow or brown
Specific Gravity1.27
Water Solubility Immiscible with water
Sensitive Light Sensitive
BRN 1420778
InChIKeyLOYZVRIHVZEDMW-UHFFFAOYSA-N
CAS DataBase Reference870-63-3(CAS DataBase Reference)
NIST Chemistry Reference2-Butene, 1-bromo-3-methyl-(870-63-3)
EPA Substance Registry System2-Butene, 1-bromo-3-methyl- (870-63-3)
Safety Information
Hazard Codes C,F
Risk Statements 10-34-20/21/22-11
Safety Statements 26-36/37/39-45-16
RIDADR UN 2920 8/PG 2
WGK Germany 3
8-10-19-23
TSCA Yes
HazardClass 3
PackingGroup III
HS Code 29033990
MSDS Information
ProviderLanguage
1-Bromo-3-methyl-2-butene English
SigmaAldrich English
ACROS English
ALFA English
3,3-Dimethylallyl bromide Usage And Synthesis
Chemical Properties3,3-Dimethylallyl bromide is colourless liquid
Uses3,3-Dimethylallyl bromide is a useful source of the 3,3-dimethylallyl or prenyl group for the synthesis of natural products1 and in the synthesis of base-modified pyrimidine nucleosides.2
Uses3,3-Dimethylallyl bromide has been used in the preparation of:
  • (±)-eldanolide
  • 1-(3,3-dimethylallyl)-L-tryptophan
  • (±)-fumagillin, antibiotic isolated from Aspergillus fumigattus
Uses3,3-Dimethylallyl bromide was used in the synthesis of 1- and 2-allylic-3-methylindoles. It was also used in the synthesis of products and base-modified pyrimidine nucleosides.

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