29971-56-0

Basic information

• Product Name: 1-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-3,4,5,6-tetra-O-acetyl-sn-myo-inositol
• CAS NO: 29971-56-0
• Molecular Weight: 678.598
• Mol File: 29971-56-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-3,4,5,6-tetra-O-acetyl-sn-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-3,4,5,6-tetra-O-acetyl-sn-myo-inositol(29971-56-0)
• EPA Substance Registry System: 1-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-3,4,5,6-tetra-O-acetyl-sn-myo-inositol(29971-56-0)

Safety Data

• Hazardous Substances Data: 29971-56-0(Hazardous Substances Data)

Upstream product

• 80065-84-5 1(3)-O-β-benzoylpropionyl-3(1),4(6),5,6(4)-tetra-O-acetyl-sn-myoinositol 
• 13462-79-8 1⁽³⁾,4⁽⁶⁾,5,6⁽⁴⁾-tetra-O-acetyl-sn-myo-inositol 
• 28140-37-6 3,4,6-tri-O-acetyl-1,2-O-(1-ethoxyethylidene)-β-D-mannopyranoside 
• 80065-86-7 1(3)-O-(β-benzoylpropionyl)-2-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-3(1),4(6),5,6(4)-tetra-O-acetyl-sn-myoinositol 
• 4715-05-3 3,4,6-tri-O-acetyl-α-D-glucopyranose-1,2-(t-butylorthoacetat) 

Downstream Products

• 35519-39-2 1(3),2,4(6),5,6(4)-penta-O-acetyl-sn-myoinositol 
• 35427-06-6 2,3⁽¹⁾,4⁽⁶⁾,5,6⁽⁴⁾-penta-O-acetyl-sn-myoinositol 
• 2347-99-1 1-O-α-D-mannopyranosyl-sn-myo-inositol 
• 2347-99-1 2-O-α-D-mannopyranosyl-sn-myo-inositol 
• 93238-43-8 1-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-2,3,4,5,6-penta-O-benzyl-sn-myo-inositol 
• 93238-43-8 3-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-1,2,4,5,6-penta-O-benzyl-sn-myo-inositol 
• 6587-77-5 1-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2,3,4,5,6-penta-O-acetyl-sn-myo-inositol 
• 21024-29-3 2-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-1,3,4,5,6-penta-O-acetyl-sn-myo-inositol 
• 6587-77-5 1-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3,4,5,6-penta-O-acetyl-sn-myo-inositol 
• 62138-04-9 3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-1,2,4,5,6-penta-O-acetyl-sn-myo-inositol 

Relevant articles and documents

INVESTIGATIONS IN THE REGION OF ASYMMETRICALLY SUBSTITUTED MYO-INOSITOL DERIVATIVES XXXIV. SYNTHESIS OF DIASTEREOMERIC ACETATES OF β-D-GLUCOSYL-MYO-INOSITOL AND CHIRAL MYO-INOSITOL PENTAACETATES

The glucosylation of racemic tetra- and pentaacetyl-myo-inositols by D-glucose tert-butylorthoacetate leads to a mixture of diastereomeric acetate derivatives of β-D-glucosyl-myo-inositol.Chiral pentaacetyl-myo-inositols were obtained from the synthesized

SYNTHESIS OF SUBSTITUTED 2-O-α-D-MANNOPYRANOSYLMYOINOSITOL

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