62774-16-7

Basic information

• Product Name: Benzyl 3-O-Benzyl-4,6-O-benzylidene-a-D-mannopyranoside
• Synonyms: Benzyl 3-O-Benzyl-4,6-O-benzylidene-a-D-mannopyranoside;Phenylmethyl 3-O-(Phenylmethyl)-4,6-O-(phenylmethylene))-a-D-mannopyranoside;Benzyl 3-O-Benzyl-4,6-O-benzylidene-α-D-mannopyranoside;Phenylmethyl 3-O-(Phenylmethyl)-4,6-O-(phenylmethylene))-α-D-mannopyranoside;1,3-Di-O-benzyl-4,6-O-benzylidene-a-D-mannopyranoside
• CAS NO: 62774-16-7
• Molecular Formula: C₂₇H₂₈O₆
• Molecular Weight: 448.51
• Product Categories: 13C & 2H Sugars;Carbohydrates & Derivatives
• Mol File: 62774-16-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 614.262°C at 760 mmHg
• Flash Point: 325.294°C
• Appearance: /
• Density: 1.282g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.626
• Solubility: Chloroform, Dichloromethane
• CAS DataBase Reference: Benzyl 3-O-Benzyl-4,6-O-benzylidene-a-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Benzyl 3-O-Benzyl-4,6-O-benzylidene-a-D-mannopyranoside(62774-16-7)
• EPA Substance Registry System: Benzyl 3-O-Benzyl-4,6-O-benzylidene-a-D-mannopyranoside(62774-16-7)

Safety Data

• Hazardous Substances Data: 62774-16-7(Hazardous Substances Data)

Usage

Chemical Properties

Colorless Oil

InChI:InChI=1/C27H28O6/c28-23-25(29-16-19-10-4-1-5-11-19)24-22(18-31-26(33-24)21-14-8-3-9-15-21)32-27(23)30-17-20-12-6-2-7-13-20/h1-15,22-28H,16-18H2/t22?,23?,24-,25-,26?,27+/m1/s1

Upstream product

• 65529-49-9 benzyl 2,3(R):4,6(R)-di-O-benzylidene-α-D-mannopyranoside 
• 40983-94-6 (4aR,6S,7S,8R,8aS)-6-benzyloxy-2-phenyl-4,4a,6,7,8,8a-hexahydropyrano[5,6-d][1,3]dioxine-7,8-diol 
• 100-39-0 benzyl bromide 
• 530-26-7 D-Mannose 
• 100-51-6 benzyl alcohol 
• 15548-45-5 (2S,3S,4S,5S,6R)-2-benzyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol 
• 58650-53-6 benzyl exo-2,3:4,6-di-O-benzylidene-α-D-mannopyranoside 

Downstream Products

• 121237-32-9 benzyl 3-O-benzyl-4,6-O-benzylidene-2-O-trifluoromethanesulfonyl-α-D-mannopyranoside 
• 79284-70-1 C₅₉H₆₃NO₂₃ 
• 86342-12-3 benzyl 2-O-allyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 23346-01-2 4,6-O-Benzylidene-1,2-dideoxy-D-erythro-hex-1-enopyranos-3-ulose 
• 72869-11-5 benzyl 4,6-O-benzylidene-2-deoxy-α-D-erythro-hexopyranosid-3-ulose 
• 121237-34-1 benzyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-erythro-hex-2-enopyranoside 
• 121237-33-0 (4aR,6S,7R,8S,8aR)-6,8-Bis-benzyloxy-7-chloro-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 121237-37-4 (4aR,6S,7R,8S,8aR)-6,8-Bis-benzyloxy-7-bromo-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 121237-38-5 (4aR,6S,7R,8S,8aR)-6,8-Bis-benzyloxy-7-iodo-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 121237-35-2 Benzoic acid (4aR,6S,7R,8S,8aR)-6,8-bis-benzyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 
• 80035-34-3 2-((4aR,6S,7R,8R,8aS)-6,8-Bis-benzyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-isoindole-1,3-dione 
• 79284-71-2 C₅₃H₆₃NO₂₂ 
• 86353-43-7 benzyl 2-O-allyl-3,4-di-O-benzyl-α-D-mannopyranoside 
• 86342-13-4 benzyl 2-O-allyl-3,4-di-O-benzyl-6-O-(p-toluenesulfonyl)-α-D-mannopyranoside 

Relevant articles and documents

INHIBITORS OF HEXOKINASE AND METHODS OF USE THEREOF

Provided herein are substituted substituted heterocycles useful as inhibitors of the HKII enzyme. The invention further provides pharmaceutical compositions of the compounds of the invention. The invention further provides medical uses of substituted heterocycles, for example, as antitumor agents.

Synthesis of a Tri-, a Penta-, and a Hepta-saccharide Containing Terminal N-Acetyl-β-D-lactosaminyl Residues, Part of the 'Complex-type' Carbohydrate Moiety of Glycoproteins

Silver trifluoromethanesulphonate-promoted condensation of 3,6-di-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-2-deoxy-2-phthalimido-β-D-glucopyranosyl bromide with benzyl 3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside, benzyl 3,6-di-O-ben