166592-73-0

Basic information

• Product Name: Methyl-6-O-(tert.-butyldimethylsilyl)-2,3,4-tri-O-benzyl-α-D-glucopyranoside
• Synonyms: Methyl-6-O-(tert.-butyldimethylsilyl)-2,3,4-tri-O-benzyl-α-D-glucopyranoside;Methyl 2,3,4-tri-O-benzyl-6-O-tert-butyldimethylsilyl-a-D-glucopyranoside;Methyl 6-O-[(1,1-dimethylethyl)dimethylsilyl]-2,3,4-tris-O-(phenylmethyl)-alpha-D-glucopyranoside
• CAS NO: 166592-73-0
• Molecular Formula: C34H46O6Si
• Molecular Weight: 578.817
• Product Categories: Carbohydrates
• Mol File: 166592-73-0.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 608.7±55.0 °C(Predicted)
• Appearance: /
• Density: 1.10±0.1 g/cm3(Predicted)
• CAS DataBase Reference: Methyl-6-O-(tert.-butyldimethylsilyl)-2,3,4-tri-O-benzyl-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl-6-O-(tert.-butyldimethylsilyl)-2,3,4-tri-O-benzyl-α-D-glucopyranoside(166592-73-0)
• EPA Substance Registry System: Methyl-6-O-(tert.-butyldimethylsilyl)-2,3,4-tri-O-benzyl-α-D-glucopyranoside(166592-73-0)

Safety Data

• Hazardous Substances Data: 166592-73-0(Hazardous Substances Data)

Upstream product

• 617-04-9 (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol 
• 1385089-80-4 methyl 2,3-di-O-benzyl-β-D-idopyranoside 
• 100-39-0 benzyl bromide 
• 1385089-78-0 methyl 2,3-di-O-benzyl-4,6-O-benzylidene-β-D-idopyranoside 
• 709-50-2 methyl beta-D-glucopyranoside 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 74264-88-3 6-O-tert-butyldimethylsilanyl-1-O-methyl-β-D-glucopyranoside 
• 3396-99-4 methyl α-D-galactopyranoside 
• 181480-80-8 6-O-tert-butyldimethylsilanyl-1-O-methyl-α-D-galactopyranoside 
• 74247-81-7 6-O-tert-butyldimethylsilanyl-1-O-methyl-α-D-mannopyranoside 
• 97-30-3 methyl-alpha-D-glucopyranoside 
• 53008-65-4 methyl 2,3,4-tri-O-benzyl-D-glucopyranoside 
• 63734-12-3 methyl 6-O-(tert-butyldimethylsilyl)-α-D-glucopyranoside 

Downstream Products

• 103597-23-5 methyl 2,3,4-tri-O-benzyl-6,7-dideoxy-L-glycero-α-D-gluco-oct-7-ene-1,5-pyranoside 
• 1401562-93-3 C₄₀H₄₁F₃O₈ 
• 1401562-88-6 C₄₀H₄₁F₃O₈ 
• 1401563-02-7 C₃₈H₅₂O₉Si 
• 1401563-04-9 C₄₈H₅₉F₃O₁₁Si 
• 1401563-00-5 C₄₈H₅₉F₃O₁₁Si 
• 83051-88-1 methyl 6-aldehydo-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 103597-19-9 methyl 2,3,4-tri-O-benzyl-6,7-dideoxy-D-glycero-α-D-glucooct-7-eno-1,5-pyranoside 
• 1401562-63-7 methyl 6-O-acetyl-2,3,4-tri-O-benzyl-α-D-erythro-D-gluco-octopyranoside 
• 155155-66-1 C₂₇H₂₆O₄ 
• 219586-93-3 2,3,4-Tri-O-benzyl-5,6-dideoxy-D-xylo-hex-5-enose oxime 
• 73111-27-0 (1R,5R,6R,7S,8S)-6,7,8-tri-O-benzyl-3-oxa-2-azabicyclo[3.3.0]octane-6,7,8-triol 
• 73111-37-2 ((1R)-2c-amino-3t,4c,5t-tris-benzyloxy-cyclopentyl)-methanol 
• 4356-80-3 methyl 2,3,4-tri-O-benzyl-β-D-glucopyranoside 

Relevant articles and documents

Synthesis and biological evaluation of 1,6-bis-triazole-2,3,4-tri-O-benzyl-α-D-glucopyranosides as a novel α-glucosidase inhibitor in the treatment of Type 2 diabetes

A novel series of 1,6-bis-triazole-benzyl-α-glucoside derivatives (7a-7ee) were designed, synthesized and evaluated for inhibitory activity against α-glucosidase. Most of the synthesized compounds exhibited good activity with IC50 ranging from

New class of alkynyl glycoside analogues as tyrosinase inhibitors

A new series of alkynyl glycoside analogues were designed and synthesized from cheap and a commercially available sugar by introduction of various alkynyl and alkyl groups at C-1 and C-6 positions of the sugar ring. The inhibitory abilities of alkynyl gly

A novel O-fucosylation strategy preactivated by (p-Tol)2SO/Tf2O and its application for the synthesis of Lewis blood group antigen Lewisa

Based on a preactivation strategy using (p-Tol)2SO/Tf2O, a new O-fucosylation method with thioglycoside as donor under mild conditions was reported. High yields and excellent α-stereoselectivities of the fucosylation were obtained wi