Cas 117300-07-9,2-C-(L-threo-3'-acetoxy-1'-benzyloxy-2'-methylpropane-1',2'-diyl)-4,6-di-O-acetyl-3-O-benzyl-2-deoxy-α-D-glucopyranoside

117300-07-9

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Basic information

Product Name: 2-C-(L-threo-3'-acetoxy-1'-benzyloxy-2'-methylpropane-1',2'-diyl)-4,6-di-O-acetyl-3-O-benzyl-2-deoxy-α-D-glucopyranoside
Synonyms: 2-C-(L-threo-3'-acetoxy-1'-benzyloxy-2'-methylpropane-1',2'-diyl)-4,6-di-O-acetyl-3-O-benzyl-2-deoxy-α-D-glucopyranoside
CAS NO:117300-07-9
Molecular Formula:
Molecular Weight: 556.61
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-C-(L-threo-3'-acetoxy-1'-benzyloxy-2'-methylpropane-1',2'-diyl)-4,6-di-O-acetyl-3-O-benzyl-2-deoxy-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 2-C-(L-threo-3'-acetoxy-1'-benzyloxy-2'-methylpropane-1',2'-diyl)-4,6-di-O-acetyl-3-O-benzyl-2-deoxy-α-D-glucopyranoside(117300-07-9)
EPA Substance Registry System: 2-C-(L-threo-3'-acetoxy-1'-benzyloxy-2'-methylpropane-1',2'-diyl)-4,6-di-O-acetyl-3-O-benzyl-2-deoxy-α-D-glucopyranoside(117300-07-9)

Safety Data

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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 117300-07-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 117300-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,3,0 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 117300-07:
(8*1)+(7*1)+(6*7)+(5*3)+(4*0)+(3*0)+(2*0)+(1*7)=79
79 % 10 = 9
So 117300-07-9 is a valid CAS Registry Number.

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117300-07-9Relevant academic research and scientific papers

STUDIES RELATED TO THE USE OF FUSED BIPYRANOSES FOR SYNTHESIS OF POLYPROPIONATE ARRAYS

Mootoo, David R.,Fraser-Reid, Bert

, p. 99 - 112 (2007/10/02)

A carbohydrate-based approach to the synthesis of polypropionate arrays (termed pyranosidic homologation) ultimately requires that the anomeric (aldehydo) group be liberated and then reduced to CH3.The bipyranose 4a has been examined in this context.Stand

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