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394521

Sigma-Aldrich

3-Bromophenethyl alcohol

99%

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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

Quality Level

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.)

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

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 Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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