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288861

Sigma-Aldrich

3-Bromophenylacetic acid

98%

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About This Item

Linear Formula:
BrC6H4CH2CO2H
CAS Number:
1878-67-7
Molecular Weight:
215.04
Beilstein:
2045104
EC Number:
217-522-1
MDL number:
MFCD00004330
UNSPSC Code:
12352100
PubChem Substance ID:
24857367
NACRES:
NA.22

Quality Level

100

Assay

98%

form

solid

mp

98-102 °C (lit.)

functional group

bromo
carboxylic acid

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

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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

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Certificates of Analysis (COA)

Lot/Batch Number
BCBZ4972
BCBX0672
BCBG2202V
BCBD8448V
MKBC5284

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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

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