881812-14-2

Basic information

• Product Name: (R,R,RS)-2,6-bis(2-biphenyl)-4-methyl-4,5-dihydro-3H-4-azacyclohepta[2,1-a;3,4a']dinaphthalene
• CAS NO: 881812-14-2
• Molecular Weight: 613.802
• Mol File: 881812-14-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R,R,RS)-2,6-bis(2-biphenyl)-4-methyl-4,5-dihydro-3H-4-azacyclohepta[2,1-a;3,4a']dinaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: (R,R,RS)-2,6-bis(2-biphenyl)-4-methyl-4,5-dihydro-3H-4-azacyclohepta[2,1-a;3,4a']dinaphthalene(881812-14-2)
• EPA Substance Registry System: (R,R,RS)-2,6-bis(2-biphenyl)-4-methyl-4,5-dihydro-3H-4-azacyclohepta[2,1-a;3,4a']dinaphthalene(881812-14-2)

Safety Data

• Hazardous Substances Data: 881812-14-2(Hazardous Substances Data)

Upstream product

• 4688-76-0 2-Biphenylboronic acid 
• 746-46-3 (R)-1,1'-binaphthyl-2,2'-dicarboxylic acid 

Relevant articles and documents

Asymmetric Strecker reaction of aldimines using aqueous potassium cyanide by phase-transfer catalysis of chiral quaternary ammonium salts with a tetranaphthyl backbone

The phase-transfer-catalyzed, highly enantioselective cyanation of aldimines using aqueous KCN has been realized based on the molecular design of chiral quaternary ammonium iodide 2c bearing a stereochemically defined tetranaphthyl backbone. For example,