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173452

4-(Phenylazo)benzoyl chloride

97%

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About This Item

Linear Formula:
C6H5N=NC6H4COCl
CAS Number:
104-24-5
Molecular Weight:
244.68
NACRES:
NA.22
PubChem Substance ID:
24850445
UNSPSC Code:
12352100
EC Number:
203-188-4
MDL number:
MFCD00041722
Assay:
97%
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assay

97%

mp

94-97 °C (lit.)

SMILES string

ClC(=O)c1ccc(cc1)\N=N\c2ccccc2

InChI

1S/C13H9ClN2O/c14-13(17)10-6-8-12(9-7-10)16-15-11-4-2-1-3-5-11/h1-9H/b16-15+

InChI key

RYMHZBAYPLCCAC-FOCLMDBBSA-N

Application

4-(Phenylazo)benzoyl chloride was used in the synthesis of polyacetylene derivatives.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKCH2521
03026HH
16523ED
10701MR
18521CB

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Antje Modrow et al.
Dalton transactions (Cambridge, England : 2003), 41(28), 8690-8696 (2012-06-14)
For the first time an azo functionality was covalently introduced into a MOF by post-synthetic modification. The reaction of Cr-MIL-101-NH(2) with p-phenylazobenzoylchloride (1) and 4-(phenylazo)phenylisocyanate (2) as the reactants led to the compounds Cr-MIL-101_amide and Cr-MIL-101_urea, with the azo groups
Yeong-Soon Gal et al.
Journal of nanoscience and nanotechnology, 11(8), 7386-7389 (2011-11-23)
A new polyacetylene derivative was prepared by the activated polymerization of 2-ethynylpyridine by using 4-(phenylazo)benzoyl chloride without any additional initiator or catalyst in high yield. The chemical structure of poly[2-ethynyl-N-(4-(phenylazo)benzoyl) pyridinium chloride [PEPABPC] was characterized by such instrumental methods as
Santanu Mondal et al.
ACS chemical biology, 13(4), 1057-1065 (2018-03-09)
Protein arginine deiminases (PADs) play an important role in the pathogenesis of various diseases, including rheumatoid arthritis, multiple sclerosis, lupus, ulcerative colitis, and breast cancer. Therefore, the development of PAD inhibitors has drawn significant research interest in recent years. Herein
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Global Trade Item Number

SKUGTIN
173452-1G04061825770659