1532592-34-9

Basic information

• Product Name: (5S,11S)-methyl2-(2,8-dimethyl-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-yl)acetate
• CAS NO: 1532592-34-9
• Molecular Weight: 322.407
• Mol File: 1532592-34-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (5S,11S)-methyl2-(2,8-dimethyl-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-yl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (5S,11S)-methyl2-(2,8-dimethyl-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-yl)acetate(1532592-34-9)
• EPA Substance Registry System: (5S,11S)-methyl2-(2,8-dimethyl-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-yl)acetate(1532592-34-9)

Safety Data

• Hazardous Substances Data: 1532592-34-9(Hazardous Substances Data)

Upstream product

• 1532592-38-3 (3aR,8aS)-3-(2-(2,8-dimethyl-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-yl)acetyl)-3,3a,8,8a-tetrahydro-2H-indeno[1,2-d]oxazol-2-one 
• 124-41-4 sodium methylate 
• 93018-88-3 2,8-dimethyl-5,6,11,12-tetrahydrodibenzo[b,f][1,5]diazocine 
• 1532592-27-0 (3aR,8aS)-3-propioloyl-3,3a,8,8a-tetrahydro-2H-indeno[1,2-d]oxazol-2-one 

Relevant articles and documents

Asymmetric synthesis of N-stereogenic molecules: Diastereoselective double aza-Michael reaction

A novel approach towards the asymmetric synthesis of N-stereogenic molecules via double aza-Michael addition was developed. The diastereomeric ratio can be increased by a thermodynamically controlled isomerization mechanism. Simple separation and functionalization of the products afford N-stereogenic compounds in high enantiomeric purity.