1402155-11-6

Basic information

• Product Name: 1-O-benzyl-5-amino-5-cyano-5-deoxy-2,3-O-(1-methylethylidene)-β-L-erythro-pentofuranose
• Synonyms: 1-O-benzyl-5-amino-5-cyano-5-deoxy-2,3-O-(1-methylethylidene)-β-L-erythro-pentofuranose
• CAS NO: 1402155-11-6
• Molecular Weight: 304.346
• Mol File: 1402155-11-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-O-benzyl-5-amino-5-cyano-5-deoxy-2,3-O-(1-methylethylidene)-β-L-erythro-pentofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-benzyl-5-amino-5-cyano-5-deoxy-2,3-O-(1-methylethylidene)-β-L-erythro-pentofuranose(1402155-11-6)
• EPA Substance Registry System: 1-O-benzyl-5-amino-5-cyano-5-deoxy-2,3-O-(1-methylethylidene)-β-L-erythro-pentofuranose(1402155-11-6)

Safety Data

• Hazardous Substances Data: 1402155-11-6(Hazardous Substances Data)

Upstream product

• 7677-24-9 trimethylsilyl cyanide 
• 102919-04-0 benzyl 2,3-O-isopropylidene-α-D-lyxo-pentodialdo-1,4-furanoside 

Relevant articles and documents

Double reductive amination and selective strecker reaction of a D-lyxaric aldehyde: Synthesis of diversely functionalized 3,4,5-trihydroxypiperidines

A D-mannose-derived aldehyde with the D-lyxo configuration is a versatile key intermediate to functionally and stereochemically diversified piperidines. It allowed the synthesis of natural 3,4,5-trihydroxypiperidines and new analogs through a double reductive amination strategy and the synthesis of novel 2-cyanotrihydroxypiperidines through a highly regio-and diastereoselective Strecker reaction.