Skip to Content
Merck
All Photos(1)

Key Documents

139726

Sigma-Aldrich

Benzoyl bromide

97%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6H5COBr
CAS Number:
Molecular Weight:
185.02
Beilstein:
1855439
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.589 (lit.)

bp

218-219 °C (lit.)

density

1.57 g/mL at 25 °C (lit.)

functional group

acyl bromide

SMILES string

BrC(=O)c1ccccc1

InChI

1S/C7H5BrO/c8-7(9)6-4-2-1-3-5-6/h1-5H

InChI key

AQIHMSVIAGNIDM-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Benzoyl bromide is a versatile reagent which causes the benzoylation of ethers.

Application

Benzoyl bromide was used to study the kinetics of solvolysis of benzoyl halides in microemulsions of sodium bis(2-ethylhexyl)sulfosuccinate/isooctane/water at 25°C.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

Supplementary Hazards

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

194.0 °F - closed cup

Flash Point(C)

90 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

Mai Do et al.
Nanoscale, 11(37), 17262-17269 (2019-06-28)
Perovskite nanoparticles have attracted the attention of research groups around the world for their impressive photophysical properties, facile synthesis and versatile surface chemistry. Here, we report a synthetic route that takes advantage of a suite of soluble precursors to generate
Tülay Polat et al.
Carbohydrate research, 338(5), 447-449 (2003-02-01)
A simple and efficient method is developed for the chemoselective one-pot conversion of ethers (benzyl, TBDMS and acetal) to the corresponding benzoates by zinc triflate-catalyzed deprotection and benzoylation by benzoyl bromide. In the same reaction, methyl or p-methoxyphenyl glycosides are
L García-Río et al.
Langmuir : the ACS journal of surfaces and colloids, 22(18), 7499-7506 (2006-08-23)
A study was carried out on the solvolysis reactions of different benzoyl halides in microemulsions of water/NH4DEHP/isooctane, where NH4DEHP is ammonium bis(2-ethylhexyl) phosphate. Because of the low solubility of benzoyl halides in water, they are distributed between the continuous medium
Dmitry Baranov et al.
ACS nano, 15(1), 650-664 (2020-12-23)
Excitonic coupling, electronic coupling, and cooperative interactions in self-assembled lead halide perovskite nanocrystals were reported to give rise to a red-shifted collective emission peak with accelerated dynamics. Here we report that similar spectroscopic features could appear as a result of

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