Skip to Content
Merck
CN

139726

Benzoyl bromide

97%

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
C6H5COBr
CAS Number:
618-32-6
Molecular Weight:
185.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848428
EC Number:
210-544-2
Beilstein/REAXYS Number:
1855439
MDL number:
MFCD00000112

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Benzoyl bromide, 97%

InChI key

AQIHMSVIAGNIDM-UHFFFAOYSA-N

InChI

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

SMILES string

BrC(=O)c1ccccc1

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
phenyl

Quality Level

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

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
GHS05,GHS07

signalword

Danger

hcodes

H314,H335

Hazard Classifications

Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

supp_hazards

EUH014

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

194.0 °F - closed cup

flash_point_c

90 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCN2585
BCCN2587
BCCK1225
BCCG2876
BCCJ2762

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

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
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
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