591727-19-4

Basic information

• Product Name: 1-2,5-6 di-O-isopropylidene 3-O-benzyl α(D)gluco-pentoaldofuranose
• Synonyms: 1-2,5-6 di-O-isopropylidene 3-O-benzyl α(D)gluco-pentoaldofuranose
• CAS NO: 591727-19-4
• Molecular Weight: 350.412
• Mol File: 591727-19-4.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: 1-2,5-6 di-O-isopropylidene 3-O-benzyl α(D)gluco-pentoaldofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1-2,5-6 di-O-isopropylidene 3-O-benzyl α(D)gluco-pentoaldofuranose(591727-19-4)
• EPA Substance Registry System: 1-2,5-6 di-O-isopropylidene 3-O-benzyl α(D)gluco-pentoaldofuranose(591727-19-4)

Safety Data

• Hazardous Substances Data: 591727-19-4(Hazardous Substances Data)

Upstream product

• 492-62-6 alpha-D-glucopyranose 
• 50-99-7 D-glucose 
• 350255-13-9 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 

Downstream Products

• 30572-04-4 1,2,4,6-tetra-O-benzoyl-3-O-benzyl-β-D-glucopyranoside 
• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 76419-48-2 methyl 4,6-O-benzylidene-3-O-benzyl-α-D-glucopyranoside 
• 35016-92-3 (3aR,5S,6R,6aR)-6-(benzyloxy)-N-hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxole-5-carbimidoyl chloride 
• 26928-32-5 3-O-benzyl-5-deoxy-1,2-O-isopropylidene-5-oximino-α-D-xylofuranose 
• 72277-35-1 (1R,2R,3S,4R)-methyl [3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-α-D-gluco]heptfuran-5-enuronate 
• 39686-94-7 3-O-benzyl-1,2,4,6-tetra-O-acetyl-D-glucopyranose 
• 247025-10-1 3-Azido-3-deoxy-4-C-hydroxymethyl-1,2-O-isopropylidene-α-D-erythro-pentofuranose 

Relevant articles and documents

Thermal analysis of new glycopolymers derived from monosaccharides

A novel monomer carrying carbohydrate moiety was prepared by simple reaction of methacrylic acid with 3-O-(2′,3′-epoxy-propyl)-1,2:5,6- di-O-isopropylidene-α-d-glucofuranose. Another d-glucose oligomer was synthesized by the polycondensation of a dicarbox

Metal-free [3+2] cycloaddition of glycosyl olefinic ester with in situ generated CF3CHN2: Access to CF3-substituted pyrazoline glycoconjugates

An efficient [3 + 2] cycloaddition of glycosyl olefinic ester with in situ generated CF3CHN2 for the syntheses of CF3-substituted pyrazoline glycoconjugate has been developed. This mild, one-pot reaction condition avoiding the use of metallic catalyst and additive will be useful in the pharmaceutical industry. This reaction features are the broad substrate scope, good functional group tolerance with good to high yields.

MODIFIED NUCLEOSIDE PHOSPHORAMIDITES

The present disclosure relates to compounds and compositions containing 5'-phosphoramidite nucleoside monomers of formulae (I) and (II), and methods of making and use, wherein the substituents are as defined in the appended claims.