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Merck
CN

394521

3-Bromophenethyl alcohol

99%

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About This Item

Linear Formula:
BrC6H4CH2CH2OH
CAS Number:
Molecular Weight:
201.06
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
liquid
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InChI

1S/C8H9BrO/c9-8-3-1-2-7(6-8)4-5-10/h1-3,6,10H,4-5H2

SMILES string

OCCc1cccc(Br)c1

InChI key

PTTFLKHCSZSFOL-UHFFFAOYSA-N

assay

99%

form

liquid

refractive index

n20/D 1.5732 (lit.)

bp

107-110 °C/1 mmHg (lit.)

density

1.478 g/mL at 25 °C (lit.)

functional group

bromo, hydroxyl

Quality Level

General description

3-Bromophenethyl alcohol is a phenethyl alcohol derivative. Its enthalpy of vaporization at boiling point has been determined.

Application

3-Bromophenethyl alcohol may be used as a starting material in the synthesis of its mesylate derivative (m-Br-C6H4CH2CH2OMs) by treatment with mesyl chloride.

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves


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Annie Tam et al.
Bioorganic & medicinal chemistry, 17(3), 1055-1063 (2008-03-04)
The traceless Staudinger ligation can be mediated by phosphinothiols under physiological conditions. Proximal positive charges are necessary to achieve that transformation, presumably because those charges discourage protonation of the key iminophosphorane intermediate. Here, a series of cationic phosphinothiols is used
Yaws CL.
Thermophysical Properties of Chemicals and Hydrocarbons, 466-466 (2008)

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