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About This Item
Linear Formula:
BrC6H4CH2CO2H
CAS Number:
Molecular Weight:
215.04
Beilstein/REAXYS Number:
2045104
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
98%
form
solid
mp
98-102 °C (lit.)
functional group
bromo
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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Related Categories
Application
3-Bromophenylacetic acid was used in the preparation of 3-bromophenylacetaldehyde by di-isobutyl aluminum hydride (DIBAL) reduction.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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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