30482-01-0

Basic information

• Product Name: 3-(2H-benzo[d][1,2,3]triazol-2-yl)-1-phenylpropan-1-one
• Synonyms: 3-(2H-benzo[d][1,2,3]triazol-2-yl)-1-phenylpropan-1-one
• CAS NO: 30482-01-0
• Molecular Weight: 251.288
• Mol File: 30482-01-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(2H-benzo[d][1,2,3]triazol-2-yl)-1-phenylpropan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2H-benzo[d][1,2,3]triazol-2-yl)-1-phenylpropan-1-one(30482-01-0)
• EPA Substance Registry System: 3-(2H-benzo[d][1,2,3]triazol-2-yl)-1-phenylpropan-1-one(30482-01-0)

Safety Data

• Hazardous Substances Data: 30482-01-0(Hazardous Substances Data)

Upstream product

• 98-86-2 acetophenone 
• 95-14-7 1,2,3-Benzotriazole 
• 1020-16-2 3-morpholino-1-phenylpropan-1-one hydrochloride 

Relevant articles and documents

An efficient water-mediated synthetic route for the alkylation of heteroarenes

An efficient synthetic route has been described for the alkylation of 1H-indole, 1H-benzimidazole, and 1H-benzotriazole. This approach features the alkylation of heteroaromatics through in situ generated enones from ketonic Mannich bases under metal-free conditions. A series of alkylated heteroaromatics have been synthesized via the K10 catalyzed alkylation reactions of these heteroaromatics with a variety of ketonic Mannich bases. Environmentally benign K10 catalyst, water-mediated mild reaction conditions, and the efficient synthesis of alkylated products are the advantages of this alkylation method.