173452
4-(Phenylazo)benzoyl chloride
97%
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About This Item
Fórmula lineal:
C6H5N=NC6H4COCl
Número de CAS:
Peso molecular:
244.68
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
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.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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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
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