74032-91-0

Basic information

• Product Name: p-nitrophenyl α-D-fucopyranoside
• Synonyms: p-nitrophenyl α-D-fucopyranoside
• CAS NO: 74032-91-0
• Molecular Weight: 285.254
• Mol File: 74032-91-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: p-nitrophenyl α-D-fucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: p-nitrophenyl α-D-fucopyranoside(74032-91-0)
• EPA Substance Registry System: p-nitrophenyl α-D-fucopyranoside(74032-91-0)

Safety Data

• Hazardous Substances Data: 74032-91-0(Hazardous Substances Data)

Upstream product

• 18992-37-5 4-nitrophenyl-2,3,4,6-tetra-O-acetyl-α-L-rhamnopyranoside 
• 51921-33-6 1,2,3,4-tetra-O-acetyl-D-fucopyranose 
• 73-34-7 D-Fucose 
• 264610-69-7 p-nitrophenyl 2,3,4-tri-O-acetyl-α-D-fucopyranoside 
• 100-02-7 4-nitro-phenol 
• 5160-09-8 2,3,4‐tri‐O‐acetyl-α-L‐rhamnopyranosyl chloride 

Downstream Products

• 100-02-7 4-nitro-phenol 
• 73-34-7 D-Fucose 
• 183879-03-0 p-nitrophenyl 3-O-methoxycarbonylmethyl-α-L-rhamnoside 
• 6014-42-2 L-rhamnose 
• 1604814-89-2 p-nitrophenyl β-D-galactofuranosyl-(1→4)-α-L-rhamnopyranoside 
• 3615-41-6 L-Rhamnose 
• 1402245-81-1 C₁₈H₂₅NO₁₂ 
• 86795-40-6 p-nitrophenyl 2-O-acetyl-4-O-benzyl-3-O-(2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside 
• 86795-41-7 p-aminophenyl 2-O-acetyl-3-O-α-L-rhamnopyranosyl-α-L-rhamnopyranoside 
• 86795-37-1 p-nitrophenyl 2-O-acetyl-4-O-benzyl-α-L-rhamnopyranoside 
• 88043-72-5 p-trifluoroacetamidophenyl 2,3-O-isopropylidene-4-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-α-L-rhamnopyranoside 
• 88043-71-4 p-nitrophenyl 2,3-O-isopropylidene-4-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-α-L-rhamnopyranoside 
• 88043-73-6 p-trifluoroacetamidophenyl 4-O-α-D-glucopyranosyl-α-L-rhamnopyranoside 
• 114284-03-6 p-nitrophenyl 4-O-(3,6-di-O-acetyl-2,4-di-O-benzyl-α-D-glucopyranosyl)-2,3-O-isopropylidene-α-L-rhamnopyranoside 

Relevant articles and documents

Synthesis of aryl α-O-L-rhamnopyranoside by two-step reaction in one pot

The title compounds were conveniently synthesized by a phase transfer catalyzed approach in two steps and one pot using the rhamnopyranosyl chloride as key intermediate. The twostep one-pot procedure is more convenient and environmentally friendly, compared to the published synthetic routes. Besides, the structure-reactivity relationship and the plausible mechanism for this base-catalyzed glycosylation were discussed bymeans of the Hammett equation.