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139726

Benzoyl bromide

97%

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About This Item

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

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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

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

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1 of 4

This Item
B17905529990429120
Benzoyl bromide 97%

Sigma-Aldrich

139726

Benzoyl bromide

Benzyl bromide reagent grade, 98%

Sigma-Aldrich

B17905

Benzyl bromide

4-Bromomethyl benzoyl bromide 96%

Sigma-Aldrich

529990

4-Bromomethyl benzoyl bromide

3-Methoxybenzyl bromide 98%

Sigma-Aldrich

429120

3-Methoxybenzyl bromide

assay

97%

assay

98%

assay

96%

assay

98%

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

100

density

1.57 g/mL at 25 °C (lit.)

density

1.438 g/mL at 25 °C (lit.)

density

-

density

1.436 g/mL at 25 °C (lit.)

bp

218-219 °C (lit.)

bp

198-199 °C (lit.)

bp

100-112 °C/0.5 mmHg (lit.)

bp

152 °C (lit.)

refractive index

n20/D 1.589 (lit.)

refractive index

n20/D 1.575 (lit.)

refractive index

-

refractive index

n20/D 1.575 (lit.)

functional group

acyl bromide

functional group

-

functional group

acyl bromide, bromo

functional group

bromo

General description

Benzoyl bromide is a versatile reagent which causes the benzoylation of ethers[1].

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[2].

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_germany

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN2585
BCCN2587
BCCK1225
BCCG2876
BCCJ2762

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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
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
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

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