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B75859

Sigma-Aldrich

α-Bromophenylacetic acid

98%

Synonym(s):

alpha-Bromophenylacetic acid

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About This Item

Linear Formula:
C6H5CH(Br)CO2H
CAS Number:
4870-65-9
Molecular Weight:
215.04
EC Number:
225-477-4
MDL number:
MFCD00004206
UNSPSC Code:
12352100
PubChem Substance ID:
24892009
NACRES:
NA.22

Quality Level

100

assay

98%

form

powder

mp

82-83 °C (lit.)

SMILES string

OC(=O)C(Br)c1ccccc1

InChI

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

InChI key

WAKFRZBXTKUFIW-UHFFFAOYSA-N

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Application

α-Bromophenylacetic acid can be used as a reactant to prepare:
  • Polymandelide by reacting with triethylamine.
  • α-Mercaptophenylacetic acid by treating with sodium hydrosulfide (NaSH·H2O).
  • β-Lactams by reacting with imines in the presence of triphenylphosphine as a mediator.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

8A - Combustible, corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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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Haihui Li et al.
Polymers, 12(1) (2020-01-16)
Polymerization-induced self-assembly (PISA) has become an effective strategy to synthesize high solid content polymeric nanoparticles with various morphologies in situ. In this work, one-step PISA was achieved by in situ photocontrolled bromine-iodine transformation reversible-deactivation radical polymerization (hereinafter referred to as
Novel Method for the Synthesis of ?-Lactams by the Reaction of ?-Bromocarboxylic Acids with Imines Mediated by Triphenylphosphine
Kikuchi S and Hashimoto Y
Heterocycles, 68(3), 453-457 (2006)
Reactions of ?-mercaptocarboxylic acid hydrazides with triethyl orthoesters: synthesis of 1, 3, 4-thiadiazin-5 (6H)-ones and 1, 3, 4-oxadiazoles
Kudelko A
Tetrahedron, 68(18), 3616-3625 (2012)

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