Cas 124485-18-3,2-O-(6-O-benzyl-2,3,4-trideoxy-α-L-glycero-hex-2-enopyranosyl)-1,3,4,6-tetra-O-acetyl-β-D-mannopyranose

124485-18-3

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Basic information

Product Name: 2-O-(6-O-benzyl-2,3,4-trideoxy-α-L-glycero-hex-2-enopyranosyl)-1,3,4,6-tetra-O-acetyl-β-D-mannopyranose
Synonyms:
CAS NO:124485-18-3
Molecular Formula:
Molecular Weight: 550.56
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-O-(6-O-benzyl-2,3,4-trideoxy-α-L-glycero-hex-2-enopyranosyl)-1,3,4,6-tetra-O-acetyl-β-D-mannopyranose(CAS DataBase Reference)
NIST Chemistry Reference: 2-O-(6-O-benzyl-2,3,4-trideoxy-α-L-glycero-hex-2-enopyranosyl)-1,3,4,6-tetra-O-acetyl-β-D-mannopyranose(124485-18-3)
EPA Substance Registry System: 2-O-(6-O-benzyl-2,3,4-trideoxy-α-L-glycero-hex-2-enopyranosyl)-1,3,4,6-tetra-O-acetyl-β-D-mannopyranose(124485-18-3)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 124485-18-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124485-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,8 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 124485-18:
(8*1)+(7*2)+(6*4)+(5*4)+(4*8)+(3*5)+(2*1)+(1*8)=123
123 % 10 = 3
So 124485-18-3 is a valid CAS Registry Number.

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124485-18-3Relevant academic research and scientific papers

Displacement of the Anomeric Alkyl Group in Racemic Methyl 2,3,4-Trideoxy-glycero-hex-2-enopyranosides by Sugar Units: Syntheses of Enantiomeric Pair of α-D-D-, α-L-D-, and α-L-L-Disaccharides

Banaszek, Anna

, p. 277 - 283 (2007/10/02)

SnCl4-catalysed coupling of the title compounds with substituted D- and L-monosaccharides possessing single OH group free at position 2,3,4 or 6 is presented.The reaction leads to 1:1 mixture of two enantiomeric diasaccharides with D- and L-configuration

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