1600532-65-7

Basic information

• Product Name: (2S,3S,4R)-1-(4-methoxyphenethyl)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)piperidine
• Synonyms: (2S,3S,4R)-1-(4-methoxyphenethyl)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)piperidine
• CAS NO: 1600532-65-7
• Molecular Weight: 551.726
• Mol File: 1600532-65-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,3S,4R)-1-(4-methoxyphenethyl)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)piperidine(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S,4R)-1-(4-methoxyphenethyl)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)piperidine(1600532-65-7)
• EPA Substance Registry System: (2S,3S,4R)-1-(4-methoxyphenethyl)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)piperidine(1600532-65-7)

Safety Data

• Hazardous Substances Data: 1600532-65-7(Hazardous Substances Data)

Upstream product

• 1421782-15-1 (2R,3R,4R)-1,3,4-tris(benzyloxy)hexane-2,5-diethylsulfonate 
• 55-81-2 4-Methoxyphenethylamine 
• 911141-04-3 (3R,4S,5R)-3,4,6-tris(benzyloxy)hexane-1,5-diol 

Downstream Products

• 1600532-87-3 (2S,3S,4R)-1-(4-methoxyphenethyl)-2-(hydroxymethyl)piperidine-3,4-diol 

Relevant articles and documents

A concise synthesis of N-substituted fagomine derivatives and the systematic exploration of their α-glycosidase inhibition

A novel and concise scheme has been developed successfully for the syntheses of N-substituted fagomine derivatives. The transformation of lactone (2) to 1,5-diol (3) was carried on with high yield (93-95%). The cyclization of 4 to 5 is a high stereoselect