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Merck
CN

135615

2-Bromo-2-methylpropane

98%

Synonym(s):

2-methyl-2-bromopropane, tert-Butyl bromide

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About This Item

Linear Formula:
(CH3)3CBr
CAS Number:
Molecular Weight:
137.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-065-9
Beilstein/REAXYS Number:
1730892
MDL number:
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Product Name

2-Bromo-2-methylpropane, 98%

InChI key

RKSOPLXZQNSWAS-UHFFFAOYSA-N

InChI

1S/C4H9Br/c1-4(2,3)5/h1-3H3

SMILES string

CC(C)(C)Br

assay

98%

form

liquid

contains

0.5% potassium carbonate as stabilizer

refractive index

n20/D 1.4279 (lit.)

bp

71-73 °C (lit.)

mp

−20 °C (lit.)

solubility

H2O: insoluble
organic solvents: miscible

density

1.22 g/mL at 20 °C (lit.)

functional group

alkyl halide
bromo

Quality Level

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Application

2-Bromo-2-methylpropane was used to study the massive deadenylation of adenine based-nucleosides induced by halogenated alkanes under physiological conditions.

General description

2-Bromo-2-methylpropane (tert-Butyl bromide) is a versatile reactant in organic synthesis, facilitating the introduction of the tert-butyl group. It causes the massive deguanylation of guanine based-nucleosides and massive deadenylation of adenine based-nucleosides.

pictograms

Flame

signalword

Danger

hcodes

Hazard Classifications

Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

60.8 °F - closed cup

flash_point_c

16 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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Deadenylation of Adenine Based-Nucleosides and Calf thymus DNA Induced by Halogenated Alkanes at the Physiological Condition.
Sherchan J, et al.
Bull. Korean Chem. Soc., 30(10), 2318-2328 (2009)
tert-Butyl Bromide-Promoted Intramolecular Cyclization of 2-Arylamino Phenyl Ketones and Its Combination with Cu-Catalyzed C-N Coupling: Synthesis of Acridines at Room Temperature
Z Cao, et al.
The Journal of Organic Chemistry, 85, 10167-10174 (2020)
Deguanylation of guanine based-nucleosides and calf thymus DNA induced by halogenated alkanes at the physiological condition.
Sherchan J and Lee E-S.
Bull. Korean Chem. Soc., 30(12), 2318-2328 (2009)

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