345830
3-Bromo-2-methylpropene
97%
Synonym(s):
Methallyl bromide, Methylallyl bromide
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About This Item
Linear Formula:
H2C=C(CH3)CH2Br
CAS Number:
Molecular Weight:
135.00
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
form
liquid
impurities
0.1% hydroquinone
refractive index
n20/D 1.472 (lit.)
bp
94-95 °C (lit.)
density
1.339 g/mL at 25 °C (lit.)
functional group
alkyl halide
bromo
storage temp.
2-8°C
SMILES string
CC(=C)CBr
InChI
1S/C4H7Br/c1-4(2)3-5/h1,3H2,2H3
InChI key
USEGQJLHQSTGHW-UHFFFAOYSA-N
General description
Rotational isomerism in 3-bromo-2-methylpropene has been studied by IR spectroscopy.
Application
3-Bromo-2-methylpropene may be used:
- in the synthesis of alkenyl imines
- in the synthesis of 2-methylpropenyl (“methallyl”) complex, Cp*Os(η3-allyl)Br2
- in a study of chiral phase transfer alkylation leading to (S)-α-alkylcysteines
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
44.6 °F - closed cup
Flash Point(C)
7 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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The Journal of organic chemistry, 71(21), 8276-8278 (2006-10-10)
We reported efficient enantioselective synthetic methodologies for (R)-alpha-alkylcysteines and (S)-alpha-alkylcysteines. The phase-transfer catalytic alkylation of 2-phenyl-2-thiazoline-4-carboxylic acid tert-butyl ester and 2-o-biphenyl-2-thiazoline-4-carboxylic acid tert-butyl ester, in the presence of chiral catalysts (1 or 2), gave the corresponding alkylated products, which could
Synthesis of Hydride and Alkyl Compounds Containing the Cp* Os (η3-allyl) Fragment. Crystal Structures of Cp* Os (η3-C8H13) Br2 and [Cp* Os (η3-C4H7) Me (H2O)][BF4].
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Angewandte Chemie (International ed. in English), 46(16), 2899-2902 (2007-03-14)
Rotational isomerism in 3-bromo, 2-methylpropene studied by ir spectroscopy.
Diallo AO.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 36(9), 799-803 (1980)
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