912847-99-5

Basic information

• Product Name: 2-((2,3,4-tri-O-benzyl-β-D-xylopyranosyl)methyl)naphthalene
• Synonyms: 2-((2,3,4-tri-O-benzyl-β-D-xylopyranosyl)methyl)naphthalene
• CAS NO: 912847-99-5
• Molecular Weight: 544.69
• Mol File: 912847-99-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-((2,3,4-tri-O-benzyl-β-D-xylopyranosyl)methyl)naphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-((2,3,4-tri-O-benzyl-β-D-xylopyranosyl)methyl)naphthalene(912847-99-5)
• EPA Substance Registry System: 2-((2,3,4-tri-O-benzyl-β-D-xylopyranosyl)methyl)naphthalene(912847-99-5)

Safety Data

• Hazardous Substances Data: 912847-99-5(Hazardous Substances Data)

Upstream product

• 66966-07-2 α/β‐L‐glucopyranosyl‐1,2,3,4,5‐pentaacetate 
• 67337-79-5 2,3,4,6-tetra-O-acetyl-α-L-glucopyranosyl bromide 
• 141434-71-1 1,5-anhydro-L-glucitol 
• 912847-93-9 1,5-anhydro-2,3,4,6-tetra-O-benzyl-L-glucitol 
• 912847-94-0 1,5-anhydro-2,3,4-tri-O-benzyl-L-glucitol 
• 912847-92-8 tetra-O-acetyl-1,5-anhydro-L-glucitol 
• 912847-95-1 2,6-anhydro-3,4,5-tri-O-benzyl-D-glucose 
• 580-13-2 2-bromonaphthalene 

Relevant articles and documents

Synthesis of aromatic C-xylosides by position inversion of glucose

Two formally C-xylosylated analogs to 2-naphthyl β-d-xylopyranoside, which is known to initiate priming of glucosaminoglycan chains, were synthesized by a position inversion of glucose (i.e., position 1 becomes position 5). The d-C-xyloside showed priming, while the l-C-xyloside did not initiate priming.