Methyl 4,6-O-benzylidene-alpha-D-glucopyranoside, 97%
Methyl 4,6-O-benzylidene-alpha-D-glucopyranoside, 97%
Methyl 4,6-O-benzylidene-alpha-D-glucopyranoside, 97%
Thermo Scientific Chemicals

Methyl 4,6-O-benzylidene-alpha-D-glucopyranoside, 97%

CAS: 3162-96-7 | C14H18O6 | 282.292 g/mol
Quantity:
5 g
25 g
100 g
Catalog number A13418.22
also known as A13418-22
Price (JPY)
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Quantity:
100 g
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Chemical Identifiers
CAS3162-96-7
IUPAC Name6-methoxy-2-phenyl-hexahydro-2H-pyrano[3,2-d][1,3]dioxine-7,8-diol
Molecular FormulaC14H18O6
InChI KeyVVSWDMJYIDBTMV-UHFFFAOYNA-N
SMILESCOC1OC2COC(OC2C(O)C1O)C1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White
Melting Point (clear melt)161.0-170.0?C
Optical Rotation110.0 ± 0.5? (C=2 in chloroform)
FormPowder or fused solid
Assay (GC)≥96.0%
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Methyl 4,6-O-benzylidene-alpha-D-glucopyranoside, is used as a chiral building block and important intermediate in the preparation of different sugars. It is also used as an intermediate in chemical, pharmaceutical intermediate, pharmaceutical research and reagent.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Methyl 4,6-O-benzylidene-alpha-D-glucopyranoside, is used as a chiral building block and important intermediate in the preparation of different sugars. It is also used as an intermediate in chemical, pharmaceutical intermediate, pharmaceutical research and reagent.

Solubility
It is soluble in water, acetone, benzene, ethyl ether

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Recommended storage temperature: 2 - 8°C. Keep away from strong oxidizing agents.
RUO – Research Use Only
F Zhang.; CX Du.; HM Liu.; Y Zhu. A novel glycoside lactone derivative with a 2-C-unsaturated diester substituent. Acta Cryst. 2001, 57,(11), 1361-1362.