1427054-91-8

Basic information

• Product Name: 1-benzyl-5-((2,3,6,7-tetramethoxyphenanthren-9-yl)methyl)-2-pyrrolidinone
• Synonyms: 1-benzyl-5-((2,3,6,7-tetramethoxyphenanthren-9-yl)methyl)-2-pyrrolidinone
• CAS NO: 1427054-91-8
• Molecular Weight: 485.58
• Mol File: 1427054-91-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-benzyl-5-((2,3,6,7-tetramethoxyphenanthren-9-yl)methyl)-2-pyrrolidinone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-5-((2,3,6,7-tetramethoxyphenanthren-9-yl)methyl)-2-pyrrolidinone(1427054-91-8)
• EPA Substance Registry System: 1-benzyl-5-((2,3,6,7-tetramethoxyphenanthren-9-yl)methyl)-2-pyrrolidinone(1427054-91-8)

Safety Data

• Hazardous Substances Data: 1427054-91-8(Hazardous Substances Data)

Upstream product

• 1427054-96-3 1-benzyl-5-[3-(4,4',5,5'-tetramethoxybiphenyl-2-yl)-2-propynyl]-2-pyrrolidinone 
• 62012-50-4 2,2'-dibromo-4,4',5,5'-tetramethoxybiphenyl 
• 2142-06-5 1-(phenylmethyl)-2,5-pyrrolidinedione 
• 1427054-93-0 1-benzyl-5-(2-propynyl)-2-pyrrolidinone 

Downstream Products

• 1427054-95-2 1-benzyl-2-[(2,3,6,7-tetramethoxyphenanthren-9-yl)methyl]pyrrolidine 

Relevant articles and documents

Concise synthesis of tylophorine

The phenanthroindolizidine alkaloid tylophorine has been synthesized in the (R)- and racemic forms. One of the routes involves three steps from a known compound employing a Stevens rearrangement as the pivotal reaction. The phenanthrene moiety was constructed by either a base-catalyzed cyclization of 2-alkynylbiphenyls or a double Suzuki coupling of a 2,2′-dibromobiphenyl with vic-bis(pinacolatoboryl)alkene in other routes.