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186295

3-Bromobenzoic acid

Name: 3-Bromobenzoic acid
Brand: ALDRICH

98%

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About This Item

Linear Formula:

BrC₆H₄CO₂H

CAS Number:

585-76-2

Molecular Weight:

201.02

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24851212

EC Number:

209-562-3

Beilstein/REAXYS Number:

2041792

MDL number:

MFCD00002487

Assay:

98%

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Properties

Quality Level

100

assay

98%

mp

155-158 °C (lit.)

solubility

methanol: soluble 50 mg/mL, clear, colorless

functional group

bromo, carboxylic acid

SMILES string

OC(=O)c1cccc(Br)c1

InChI

1S/C7H5BrO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,(H,9,10)

InChI key

VOIZNVUXCQLQHS-UHFFFAOYSA-N

Description

Application

3-Bromobenzoic acid was used:

as test solute in the determination of acidity constants by capillary zone electrophoresis
as internal standard to study the retention mechanisms of an unmodified and a hydroxylated polystyrene-divinylbenzene polymer by solid-phase extraction
in synthesis of N-(1,1-dimethyl-2-hydroxyethyl)-3-bromobenzamide

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Analysis of mono- and diesters of o-phthalic acid by solid-phase extractions with polystyrene-divinylbenzene-based polymers.

Susanne Jonsso et al.

Journal of chromatography. A, 963(1-2), 393-400 (2002-08-22)

Retention mechanisms of an unmodified and a hydroxylated polystyrene-divinylbenzene polymer were studied by solid-phase extraction of o-phthalic acid and some of its mono- and diesters from purified water and then analysing by GC-MS. The monoesters and phthalic acid were retained

Structure-based design guides the improved efficacy of deacylation transition state analogue inhibitors of TEM-1 beta-Lactamase(,).

S Ness et al.

Biochemistry, 39(18), 5312-5321 (2000-05-23)

Transition state analogue boronic acid inhibitors mimicking the structures and interactions of good penicillin substrates for the TEM-1 beta-lactamase of Escherchia coli were designed using graphic analyses based on the enzyme's 1.7 A crystallographic structure. The synthesis of two of

Fast high-throughput method for the determination of acidity constants by capillary electrophoresis. II. Acidic internal standards.

Joan Marc Cabot et al.

Journal of chromatography. A, 1217(52), 8340-8345 (2010-11-23)

A fast method for the determination of acidity constants by CZE has been recently developed. This method is based on the use of an internal standard of pK(a) similar to that of the analyte. In this paper we establish the

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Global Trade Item Number

SKU	GTIN
186295-25G	04061838758064