Skip to Content
Merck
All Photos(1)

Key Documents

288861

Sigma-Aldrich

3-Bromophenylacetic acid

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
BrC6H4CH2CO2H
CAS Number:
Molecular Weight:
215.04
Beilstein:
2045104
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

solid

mp

98-102 °C (lit.)

SMILES string

OC(=O)Cc1cccc(Br)c1

InChI

1S/C8H7BrO2/c9-7-3-1-2-6(4-7)5-8(10)11/h1-4H,5H2,(H,10,11)

InChI key

KYNNBXCGXUOREX-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

3-Bromophenylacetic acid was used in the preparation of 3-bromophenylacetaldehyde by di-isobutyl aluminum hydride (DIBAL) reduction.

Storage Class Code

11 - Combustible Solids

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

James R Davies et al.
The Journal of organic chemistry, 70(18), 7305-7316 (2005-08-27)
[structure: see text] Various approaches to the indole bis-oxazole fragment of the marine secondary metabolite diazonamide A are described, all of which feature dirhodium(II)-catalyzed reactions of diazocarbonyl compounds in key steps. Thus, 3-bromophenylacetaldehyde is converted into an alpha-diazo-beta-ketoester, dirhodium(II)-catalyzed reaction

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service