1072913-30-4

Basic information

• Product Name: (2-amino-4,5-dimethoxyphenyl)(phenyl)methanol
• Synonyms: (2-amino-4,5-dimethoxyphenyl)(phenyl)methanol
• CAS NO: 1072913-30-4
• Molecular Weight: 259.305
• Mol File: 1072913-30-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (2-amino-4,5-dimethoxyphenyl)(phenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2-amino-4,5-dimethoxyphenyl)(phenyl)methanol(1072913-30-4)
• EPA Substance Registry System: (2-amino-4,5-dimethoxyphenyl)(phenyl)methanol(1072913-30-4)

Safety Data

• Hazardous Substances Data: 1072913-30-4(Hazardous Substances Data)

Upstream product

• 22608-87-3 2-amino-4,5-dimethoxybenzaldehyde 
• 100-58-3 phenylmagnesium bromide 
• 39996-22-0 (2-amino-4,5-dimethoxyphenyl)-(phenyl)methanone 
• 179104-60-0 α-phenyl-4,5-dimethoxy-2-nitrobenzyl alcohol 

Downstream Products

• 161493-12-5 ethyl 6,7-dimethoxy-2-methyl-4-phenylquinoline-3-carboxylate 

Relevant articles and documents

A simple route to polysubstituted indoles exploiting azide induced furan ring opening

A straightforward, efficient indole synthesis based on thermolysis of 2-(2-azidobenzyl)furans with attack of the formed nitrene moiety onto the ipso position of furan ring has been developed. The cyclization is accompanied by furan ring opening and affords indoles with a 2-acylvinyl substituent suitable for further modifications.

A novel and efficient methodology for the construction of quinazolines based on supported copper oxide nanoparticles

A series of quinazolines were synthesized from 2-aminobenzophenones and benzylic amines in good to excellent yields by employing a new heterogeneous catalyst based on the copper oxide nanoparticles supported on kaolin.