6587-77-5

Basic information

• Product Name: 1-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3,4,5,6-penta-O-acetyl-sn-myo-inositol
• CAS NO: 6587-77-5
• Molecular Weight: 720.636
• Mol File: 6587-77-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3,4,5,6-penta-O-acetyl-sn-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3,4,5,6-penta-O-acetyl-sn-myo-inositol(6587-77-5)
• EPA Substance Registry System: 1-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3,4,5,6-penta-O-acetyl-sn-myo-inositol(6587-77-5)

Safety Data

• Hazardous Substances Data: 6587-77-5(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 29971-56-0 1-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-3,4,5,6-tetra-O-acetyl-sn-myo-inositol 
• 4715-05-3 3,4,6-tri-O-acetyl-α-D-glucopyranose-1,2-(t-butylorthoacetat) 
• 5517-47-5 1⁽³⁾,2,4⁽⁶⁾,5,6⁽⁴⁾-penta-O-acetyl-sn-myo-inositol 
• 28140-37-6 3,4,6-tri-O-acetyl-1,2-O-(1-ethoxyethylidene)-β-D-mannopyranoside 
• 210281-95-1 β-D-mannopyranosyl fluoride 
• 2347-99-1 1-O-α-D-mannopyranosyl-sn-myo-inositol 
• 29971-56-0 1-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-3,4,5,6-tetra-O-acetyl-sn-myo-inositol 

Downstream Products

• 6605-49-8 α-D-mannopyranosyl-sn-myo-inositol 
• 2347-99-1 1-O-α-D-mannopyranosyl-sn-myo-inositol 
• 35519-39-2 1(3),2,4(6),5,6(4)-penta-O-acetyl-sn-myoinositol 

Relevant articles and documents

Creation of an α-mannosynthase from a broad glycosidase scaffold

α-Mannosides made easy: Mutation of a family-GH31 α-glucosidase that displays plasticity to alterations at the 2-OH position of donor substrates created an efficient α-mannoside-synthesizing biocatalyst. A simple fluoride donor reagent was used for the synthesis of a range of mono-α-mannosylated conjugates using the α-mannosynthase displaying low (unwanted) oligomerization activity. Copyright

DERIVATIVES OF ASYMMETRICALLY SUBSTITUTED MYO-INOSITOL. XXXIII. SYNTHESIS OF DIASTEROMERIC MANNOSIDES OF MYO-INOSITOL

Diastereomeric acetylated mannosides of myo-inositol were synthesized by the glycosylation of the racemic acetates of myo-inositol with the ethyl orthoacetate of D-mannose.The synthesized mannosides of myo-inositol can be used for the production of chiral myo-inositol acetates and as intermediates in the synthesis of complex phosphoinositides.