1359819-65-0

Basic information

• Product Name: (1S,2S,3R,4R,5R)-4-amino-5-methylcyclopentane-1,2,3-triol
• CAS NO: 1359819-65-0
• Molecular Weight: 147.174
• Mol File: 1359819-65-0.mol

Chemical Properties

• CAS DataBase Reference: (1S,2S,3R,4R,5R)-4-amino-5-methylcyclopentane-1,2,3-triol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S,3R,4R,5R)-4-amino-5-methylcyclopentane-1,2,3-triol(1359819-65-0)
• EPA Substance Registry System: (1S,2S,3R,4R,5R)-4-amino-5-methylcyclopentane-1,2,3-triol(1359819-65-0)

Safety Data

• Hazardous Substances Data: 1359819-65-0(Hazardous Substances Data)

Upstream product

• 1359756-33-4 (S)-N-((3aR,4R,5R,6S,6aS)-6-hydroxy-2,2,5-trimethyl-tetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)-2-methylpropane-2-sulfinamide 
• 1359756-28-7 (S)-N-((3aS,4R,6S,6aS)-2,2-dimethyl-6-vinyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-2-methylpropane-2-sulfinamide 

Relevant articles and documents

Intramolecular tandem isomerization-mannich reaction as a new route towards aminocyclopentitols

A new efficient synthetic strategy has been developed to prepare aminocyclopentitols. It is based on an iron-catalyzed tandem isomerization-Mannich reaction and uses chiral N-tert-butanesulfinamide as a chiral auxiliary. This methodology has been applied