173452
4-(Phenylazo)benzoyl chloride
97%
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About This Item
Produits recommandés
Pureté
97%
Pf
94-97 °C (lit.)
Chaîne SMILES
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+
Clé InChI
RYMHZBAYPLCCAC-FOCLMDBBSA-N
Application
4-(Phenylazo)benzoyl chloride was used in the synthesis of polyacetylene derivatives.
Mention d'avertissement
Danger
Mentions de danger
Classification des risques
Eye Dam. 1 - Skin Corr. 1B
Code de la classe de stockage
8A - Combustible corrosive hazardous materials
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
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
Journal of nanoscience and nanotechnology, 11(8), 7386-7389 (2011-11-23)
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