148431-62-3 Usage
Type of sugar molecule
Rhamnopyranose
Structural modification
Dehydration process to form the 1,2-anhydro structure
Further modification
Benzyl groups attached to the 3 and 4 hydroxyl groups
Resulting compound
Benzylrhamnopyranose
Potential applications
Organic chemistry, synthesis of natural products, and pharmaceuticals
Unique structure
Valuable building block for creating complex molecules
Importance
Contributes to the development of novel compounds and therapeutic agents
Check Digit Verification of cas no
The CAS Registry Mumber 148431-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,4,3 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 148431-62:
(8*1)+(7*4)+(6*8)+(5*4)+(4*3)+(3*1)+(2*6)+(1*2)=133
133 % 10 = 3
So 148431-62-3 is a valid CAS Registry Number.
148431-62-3Relevant articles and documents
Synthesis, conformational analysis, and the glycosidic coupling reaction of substituted 2,7-dioxabicyclo[4.1.0]heptanes: 1,2-anhydro-3,4-di-O-benzyl-β-L- and β-D-rhamnopyranoses
Chen,Kong,Cao
, p. 107 - 117 (2007/10/02)
1,2-Anhydro-3,4-di-O-benzyl-α-L-rhamnopyranose was synthesized from L-rhamnose, while the D-enantiomer was synthesized from methyl 6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside. For both of the syntheses, the key intermediates were 2-O-acetyl-3,4-di-O-
