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240540

Sigma-Aldrich

Benzoyl chloride

ReagentPlus®, ≥99%

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About This Item

Linear Formula:
C6H5COCl
CAS Number:
Molecular Weight:
140.57
Beilstein:
471389
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

vapor density

4.88 (vs air)

vapor pressure

1 mmHg ( 32 °C)

product line

ReagentPlus®

Assay

≥99%

autoignition temp.

1056 °F

expl. lim.

4.9 %

refractive index

n20/D 1.553 (lit.)

bp

198 °C (lit.)

mp

−1 °C (lit.)

density

1.211 g/mL at 25 °C (lit.)

SMILES string

ClC(=O)c1ccccc1

InChI

1S/C7H5ClO/c8-7(9)6-4-2-1-3-5-6/h1-5H

InChI key

PASDCCFISLVPSO-UHFFFAOYSA-N

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Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Skull and crossbonesCorrosion

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

Flash Point(F)

161.6 °F - closed cup

Flash Point(C)

72 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Solid catalyst treated with anion: XVIII. Benzoylation of toluene with benzoyl chloride and benzoic anhydride catalysed by solid superacid of sulfate-supported alumina.
Arata K and Hino M.
Applied Catalysis, 59(1), 197-204 (1990)
High activity of iron containing metal-organic-framework in acylation of p-xylene with benzoyl chloride.
Kurfirtova L, et al.
Catalysis Today, 179(1), 85-90 (2012)
An unexpected silver triflate-catalyzed reaction of 2-alkynylbenzaldoxime in the presence of benzoyl chloride.
Liu G, et al.
Royal Society of Chemistry Advances, 3(27), 10666-10668 (2013)
Adem Asan et al.
Journal of chromatography. A, 988(1), 145-149 (2003-03-22)
A simple reversed-phase LC method capable of detecting ng/ml quantities of phenolic compounds in water is described. Pre-column derivatization with benzoyl chloride is used for the separation and determination o-cresol, m-cresol, p-cresol, phenol, resorcinol, catechol and hydroquinone in water. The
Iterative dianion relay along the ring: formation of gem-bis(trimethylsilyl) cyclopentenones from 2,5-bis(trimethylsilyl) oxy-cyclopentadienyl dianions and acid chlorides.
Heng Li et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(27), 7399-7403 (2011-05-28)

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