1259298-27-5

Basic information

• Product Name: 4-methoxyphenyl 2,3,4-tri-O-benzyl-6-O-tert-butyldiphenylsilyl-β-D-glucopyranoside
• Synonyms: 4-methoxyphenyl 2,3,4-tri-O-benzyl-6-O-tert-butyldiphenylsilyl-β-D-glucopyranoside
• CAS NO: 1259298-27-5
• Molecular Weight: 795.06
• Mol File: 1259298-27-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-methoxyphenyl 2,3,4-tri-O-benzyl-6-O-tert-butyldiphenylsilyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxyphenyl 2,3,4-tri-O-benzyl-6-O-tert-butyldiphenylsilyl-β-D-glucopyranoside(1259298-27-5)
• EPA Substance Registry System: 4-methoxyphenyl 2,3,4-tri-O-benzyl-6-O-tert-butyldiphenylsilyl-β-D-glucopyranoside(1259298-27-5)

Safety Data

• Hazardous Substances Data: 1259298-27-5(Hazardous Substances Data)

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 1055325-21-7 p-methoxyphenyl 2,3,4-tri-O-benzyl-β-D-glucopyranoside 
• 1075709-09-9 1-O-p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-β-D-glucopyranose 
• 100-39-0 benzyl bromide 
• 3150-20-7 4-methoxyphenyl β-D-glucopyranoside 
• 150-76-5 4-methoxy-phenol 
• 2872-65-3 p-methoxyphenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 
• 604-69-3 β-D-glucose pentaacetate 

Downstream Products

• 1448001-58-8 p-methoxyphenyl 2,3-O-acetyl-6-O-benzyl-4-O-(2,3,4-tri-O-benzyl-6-O-acetyl-β-D-glusopyranosyl)-β-D-galactopyranoside 
• 1448001-59-9 2,3-O-acetyl-6-O-benzyl-4-O-(2,3,4-tri-O-benzyl-6-O-acetyl-β-D-glucopyranosyl)-β-D-galactopyranosyl N-phenyltrifluoroacetimidate 
• 1448001-78-2 C₃₉H₆₈O₁₁ 
• 88567-49-1 6-O-acetyl-2,3,4-tri-O-benzyl-D-glucopyranose 
• 1055325-21-7 p-methoxyphenyl 2,3,4-tri-O-benzyl-β-D-glucopyranoside 
• 1206803-44-2 p-methoxyphenyl 6-O-acetyl-2,3,4-tri-O-benzyl-β-D-glucopyranoside 

Relevant articles and documents

A divergent approach to the synthesis of simplexides and congeners via a late-stage olefin cross-metathesis reaction

Simplexides constitute a unique group of immunosuppressive glycolipids that demonstrate antiproliferative activities against activated T-cell lymphocytes via a unique non-cytotoxic inhibition. To investigate the structure-activity relationship of the varied long-chain secondary alcohols on simplexides, we developed an efficient and divergent route to the synthesis of simplexides and congeners, taking advantage of a late-stage olefin cross-metathesis reaction.