883104-82-3

Basic information

• Product Name: N-(6-methoxy-8-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl)-O-methyl-hydroxylamine
• CAS NO: 883104-82-3
• Molecular Weight: 309.362
• Mol File: 883104-82-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(6-methoxy-8-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl)-O-methyl-hydroxylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(6-methoxy-8-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl)-O-methyl-hydroxylamine(883104-82-3)
• EPA Substance Registry System: N-(6-methoxy-8-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl)-O-methyl-hydroxylamine(883104-82-3)

Safety Data

• Hazardous Substances Data: 883104-82-3(Hazardous Substances Data)

Upstream product

• 883104-81-2 (2R,4aR,6S,8aS)-6-Methoxy-2-phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-8-one O-methyl-oxime 
• 94616-84-9 dichloromethylcerium 

Downstream Products

• 85687-30-5 methyl 4-O-benzoyl-6-bromo-2,3,6-trideoxy-3-C-methyl-3-(trifluoroacetamido)-α-D-ribo-hexopyranoside 
• 98758-31-7 methyl 4,6-O-benzylidene-2,3-dideoxy-3-C-methyl-3-(trifluoroacetamido)-α-D-ribo-hexopyranoside 
• 95087-00-6 4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-3-trifluoroacetamido-αβ-L-lyxo-hexopyranose 
• 95086-99-0 methyl 4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-3-trifluoroacetamido-β-L-lyxohexopyranoside 
• 95086-98-9 methyl 4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-3-trifluoroacetamido-α-D-erythro-hex-5-enopyranoside 
• 883104-85-6 Benzoic acid (2S,3S,4S,6R)-6-acetoxy-2,4-dimethyl-4-(2,2,2-trifluoro-acetylamino)-tetrahydro-pyran-3-yl ester 
• 883104-83-4 2,2,2-trifluoro-N-methoxy-N-(6-methoxy-8-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl)-acetamide 

Relevant articles and documents

Synthesis of L-vancosamine derivatives from methyl α-D- mannopyranoside

Concise synthesis of L-vancosamine, the amino sugar constituent of vancomycin and other antibiotics, has been achieved. The key steps include (1) stereoselective addition of methylcerium reagent to oximino ether, and (2) stereoselective hydrogenation of 5