b-D-Glucopyranose, 1,6-anhydro-2,3,4-tris-O-(phenylmethyl)-


Chemical Name: b-D-Glucopyranose, 1,6-anhydro-2,3,4-tris-O-(phenylmethyl)-
CAS Number: 10548-46-6
Product Number: AG007EKU(AGN-PC-0OUSQB)
Synonyms:
MDL No:
Molecular Formula: C27H28O5
Molecular Weight: 432.5082

Identification/Properties


Computed Properties
Molecular Weight:
432.516g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
9
Exact Mass:
432.194g/mol
Monoisotopic Mass:
432.194g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
32
Formal Charge:
0
Complexity:
538
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
5
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



1,6-Anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose is a versatile compound that finds wide application in chemical synthesis, particularly in organic chemistry. This compound serves as a valuable building block for the synthesis of complex molecules due to its unique reactivity and structure.In chemical synthesis, 1,6-Anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose can be utilized as a protecting group for the hydroxyl groups present on the glucose ring. By selectively protecting these hydroxyl groups with benzyl groups, the compound becomes more stable and resistant to unwanted reactions during subsequent chemical transformations. This protection strategy allows chemists to control the reactivity of the hydroxyl groups, enabling selective reactions at other functional groups within a molecule.Moreover, the benzyl-protected glucose derivative can undergo various chemical reactions, such as acylation, reduction, and substitution, to introduce new functional groups or modify the sugar moiety. This flexibility in chemical transformations makes 1,6-Anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose a valuable intermediate in the synthesis of complex carbohydrates, glycosides, and natural products.Overall, the application of 1,6-Anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose in chemical synthesis highlights its importance as a strategic building block for the efficient construction of diverse organic molecules with specific structural modifications.