1075709-09-9

Basic information

• Product Name: 1-O-p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-β-D-glucopyranose
• Synonyms: 1-O-p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-β-D-glucopyranose
• CAS NO: 1075709-09-9
• Molecular Weight: 524.686
• Mol File: 1075709-09-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-O-p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-β-D-glucopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-β-D-glucopyranose(1075709-09-9)
• EPA Substance Registry System: 1-O-p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-β-D-glucopyranose(1075709-09-9)

Safety Data

• Hazardous Substances Data: 1075709-09-9(Hazardous Substances Data)

Upstream product

• 150-76-5 4-methoxy-phenol 
• 604-69-3 β-D-glucose pentaacetate 
• 572-09-8 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl bromide 
• 4336-91-8 3-bromo-2-pyridyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 
• 83-87-4 D-glucose pentaacetate 
• 2872-65-3 p-methoxyphenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 3150-20-7 4-methoxyphenyl β-D-glucopyranoside 

Downstream Products

• 1075708-82-5 4-methoxyphenyl 2,3,4-tri-O-[D7]benzyl-β-D-glucopyranoside 
• 1344980-54-6 1-O-p-methoxyphenyl 2,3,4-tri-O-benzoyl-β-D-glucopyranose 
• 1344980-48-8 1-O-p-methoxyphenyl 2,3,4-tri-O-benzoyl-6-O-tert-butyldiphenylsilyl-β-D-glucopyranose 
• 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 
• 1259298-27-5 4-methoxyphenyl 2,3,4-tri-O-benzyl-6-O-tert-butyldiphenylsilyl-β-D-glucopyranoside 

Relevant articles and documents

Tea leaf perfumery precursor glucoside and synthesizing method thereof

The invention relates to a tea leaf perfumery precursor glucoside and a synthesizing method thereof. The synthesizing method comprises the following steps of synthesizing ten glucosides including aromatic alcohol ( alkanol )-beta -D-glucosides and aromatic alcohol (alkanol )-beta -D-primrose indicans. The synthesizing method disclosed by the invention is a glucoside synthesizing method which is good in selectivity, high in production rate and low in cost.

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.

NAP ether mediated intramolecular aglycon delivery: A unified strategy for 1,2-cis-glycosylation

A methodology directed towards the stereoselective construction of 1,2-cis-glycosides through naphthylmethyl (NAP) ether mediated intramolecular aglycon derivery (IAD) has been developed. Stereospecific constructions of various 1,2-cis linkages, as in β-mannopyrano-, β-arabinofurano-, and α-glucopyranosides, were achieved through NAP-IAD. This methodology was successfully applied to the synthesis of Glcα(1→2)- Glcα(1→3)-Glcα(1→3)Man (Glc3Man1), the nonreducing terminal structure of the tetradecasaccharide Glc 3Man9GlcNAc2, a common precursor of all N-linked glycans. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.