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03-1440

Sigma-Aldrich

Benzoyl chloride

SAJ first grade, ≥98.0%

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About This Item

Fórmula lineal:
C6H5COCl
Número de CAS:
98-88-4
Peso molecular:
140.57
Beilstein/REAXYS Number:
471389
EC Number:
202-710-8
MDL number:
MFCD00000653
UNSPSC Code:
12352100
PubChem Substance ID:
329747564

grade

SAJ first grade

vapor density

4.88 (vs air)

vapor pressure

1 mmHg ( 32 °C)

assay

≥98.0%

autoignition temp.

1056 °F

expl. lim.

4.9 %

availability

available only in Japan

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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pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

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

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

wgk_germany

WGK 1

flash_point_f

161.6 °F - closed cup

flash_point_c

72 °C - closed cup

ppe

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

Certificados de análisis (COA)

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Cong Li et al.
Journal of the American Society for Mass Spectrometry, 24(4), 493-501 (2013-03-21)
The benzoxyl radical is a key intermediate in the combustion of toluene and other aromatic hydrocarbons, yet relatively little experimental work has been performed on this species. Here, a combination of electrospray ionization (ESI), multistage mass spectrometry experiments, and density
Ran Liu et al.
Journal of mass spectrometry : JMS, 47(10), 1341-1346 (2012-09-29)
A high-performance liquid chromatography coupled with Q-time of flight mass spectrometry (HPLC/Q-TOF MS) method was developed and validated for the determination of 1, 3-diaminopropane, putrescine, cadaverine, spermidine and spermine in human plasma. The plasma samples were first pretreated by 10%
Ozgül Ozdestan et al.
Talanta, 78(4-5), 1321-1326 (2009-04-14)
A new benzoylation procedure was developed which was more reliable than the most common benzoylation procedures in terms of reaction time, peak resolution, detector response and repeatability. Methylamine, putrescine, cadaverine, tryptamine, beta-phenylethylamine, spermidine, spermine, histamine, tyramine and agmatine were studied.
Russell J Cox et al.
Chemical communications (Cambridge, England), (8)(8), 1037-1039 (2005-02-19)
Conditions are reported for the facile, high-yielding coupling of acyl chlorides with terminal alkynes in a reaction involving palladium and copper iodide; the reaction is tolerant of a wide variety of acyl chlorides and terminal alkynes and provides a convenient
Vutukuri Prakash Reddy et al.
Organic & biomolecular chemistry, 13(24), 6803-6813 (2015-05-27)
The direct sulfenylation and sulfonylation of (sp(2))C-H bonds of benzamide derivatives were achieved using a Ni catalyst with the aid of an 8-aminoquinoline moiety as a bidentate directing group. These protocols represent a convenient route for the formation of valuable
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