1456629-35-8

Basic information

• Product Name: methyl 3-[1-(9,10-dioxo-9,10-dihydroanthracen-2-yl)ethyl]-5-phenyl-1H-1,2,3-triazole-4-carboxylate
• Synonyms: methyl 3-[1-(9,10-dioxo-9,10-dihydroanthracen-2-yl)ethyl]-5-phenyl-1H-1,2,3-triazole-4-carboxylate
• CAS NO: 1456629-35-8
• Molecular Weight: 437.455
• Mol File: 1456629-35-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 3-[1-(9,10-dioxo-9,10-dihydroanthracen-2-yl)ethyl]-5-phenyl-1H-1,2,3-triazole-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-[1-(9,10-dioxo-9,10-dihydroanthracen-2-yl)ethyl]-5-phenyl-1H-1,2,3-triazole-4-carboxylate(1456629-35-8)
• EPA Substance Registry System: methyl 3-[1-(9,10-dioxo-9,10-dihydroanthracen-2-yl)ethyl]-5-phenyl-1H-1,2,3-triazole-4-carboxylate(1456629-35-8)

Safety Data

• Hazardous Substances Data: 1456629-35-8(Hazardous Substances Data)

Upstream product

• 1456629-37-0 2-(1-azidoethyl)anthraquinone 
• 4891-38-7 phenylpropynoic acid methyl ester 
• 93989-43-6 2-(1-bromoethyl)anthraquinone 
• 84-51-5 2-ethylanthraquinone 

Relevant articles and documents

Synthesis of 2-substituted 9,10-anthraquinones

A convenient preparation of racemic 2-substituted 9,10-anthraquinones that included 2-triazoylethyl skeleton 1 and 2-alkylethyl skeleton 6 is reported. The products were obtained in good yields by a three-or four-step synthetic route based on a sequence of N-bromosuccinimide (NBS)-mediated bromination of 2-ethyl-9,10-anthraquinone 2, nucleophilic substitution, and CuI-catalyzed 1,3-dipolar cycloaddition or alkylation/reductive desulfonylation. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications for the following free supplemental resource(s): Full experimental and spectral details.]