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About This Item
Linear Formula:
BrC6H4CH2CH2OH
CAS Number:
Molecular Weight:
201.06
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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
SMILES string
OCCc1cccc(Br)c1
InChI
1S/C8H9BrO/c9-8-3-1-2-7(6-8)4-5-10/h1-3,6,10H,4-5H2
InChI key
PTTFLKHCSZSFOL-UHFFFAOYSA-N
Related Categories
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_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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Yaws CL.
Thermophysical Properties of Chemicals and Hydrocarbons, 466-466 (2008)
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
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