1073131-04-0

Basic information

• Product Name: (4S,5R)-N-methoxy-5-((4-methoxybenzyloxy)methyl)-N,2,2-trimethyl-1,3-dioxolane-4-carboxamide
• Synonyms: (4S,5R)-N-methoxy-5-((4-methoxybenzyloxy)methyl)-N,2,2-trimethyl-1,3-dioxolane-4-carboxamide
• CAS NO: 1073131-04-0
• Molecular Weight: 339.389
• Mol File: 1073131-04-0.mol

Chemical Properties

• CAS DataBase Reference: (4S,5R)-N-methoxy-5-((4-methoxybenzyloxy)methyl)-N,2,2-trimethyl-1,3-dioxolane-4-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5R)-N-methoxy-5-((4-methoxybenzyloxy)methyl)-N,2,2-trimethyl-1,3-dioxolane-4-carboxamide(1073131-04-0)
• EPA Substance Registry System: (4S,5R)-N-methoxy-5-((4-methoxybenzyloxy)methyl)-N,2,2-trimethyl-1,3-dioxolane-4-carboxamide(1073131-04-0)

Safety Data

• Hazardous Substances Data: 1073131-04-0(Hazardous Substances Data)

Upstream product

• 1073130-85-4 C₁₅H₂₀O₆ 
• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 

Downstream Products

• 1073130-86-5 1-((4S,5R)-5-((4-methoxybenzyloxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-methylprop-2-en-1-one 

Relevant articles and documents

L-Selectride-mediated highly diastereoselective asymmetric reductive Aldol reaction: Access to an important subunit for bioactive molecules

(Equation Presented) L-Selectride reduction of a chiral or achiral enone followed by reaction of the resulting enolate with optically active α-alkoxy aldehydes proceeded with excellent diastereoselectivity. The resulting α,α-dimethyl-β-hydroxy ketones are