Home Other Building Blocks 1,2,3,6-TETRA-O-ACETYL-ALPHA-D-GLUCOPYRANOSE

1,2,3,6-TETRA-O-ACETYL-ALPHA-D-GLUCOPYRANOSE

CAS No.:
55286-97-0
Catalog Number:
AG00DAQ1
Molecular Formula:
Molecular Weight:
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Product Description
Catalog Number:
AG00DAQ1
Chemical Name:
1,2,3,6-TETRA-O-ACETYL-ALPHA-D-GLUCOPYRANOSE
CAS Number:
55286-97-0
MDL Number:
MFCD00061639
IUPAC Name:
[(2R,3R,4S,5R,6R)-4,5,6-triacetyloxy-3-hydroxyoxan-2-yl]methyl acetate
InChI:
InChI=1S/C14H20O10/c1-6(15)20-5-10-11(19)12(21-7(2)16)13(22-8(3)17)14(24-10)23-9(4)18/h10-14,19H,5H2,1-4H3/t10-,11-,12+,13-,14+/m1/s1
InChI Key:
QYCFXXCSGBEENZ-RGDJUOJXSA-N
Properties
Complexity:
502  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
5  
Defined Bond Stereocenter Count:
0
Exact Mass:
348.106g/mol
Formal Charge:
0
Heavy Atom Count:
24  
Hydrogen Bond Acceptor Count:
10  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
348.304g/mol
Monoisotopic Mass:
348.106g/mol
Rotatable Bond Count:
9  
Topological Polar Surface Area:
135A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.1  
Literature
Title Journal
2,3,4,6-Tetra-O-acetyl-2-phthalimido-β-d-glucopyran-oside. Acta crystallographica. Section E, Structure reports online 20101201
Regioselective enzymatic hydrolysis of acetylated pyranoses and pyranosides using immobilised lipases. An easy chemoenzymatic synthesis of alpha- and beta-D-glucopyranose acetates bearing a free secondary C-4 hydroxyl group. Carbohydrate research 20021008
Properties