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About This Item
Linear Formula:
C6H5COBr
CAS Number:
Molecular Weight:
185.02
Beilstein/REAXYS Number:
1855439
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
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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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.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
supp_hazards
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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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
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