Cas 64656-22-0,3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-1,2,4,5,6-penta-O-benzyl-sn-myoinositol

64656-22-0

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Basic information

Product Name: 3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-1,2,4,5,6-penta-O-benzyl-sn-myoinositol
Synonyms:
CAS NO:64656-22-0
Molecular Formula:
Molecular Weight: 961.072
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: 3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-1,2,4,5,6-penta-O-benzyl-sn-myoinositol(CAS DataBase Reference)
NIST Chemistry Reference: 3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-1,2,4,5,6-penta-O-benzyl-sn-myoinositol(64656-22-0)
EPA Substance Registry System: 3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-1,2,4,5,6-penta-O-benzyl-sn-myoinositol(64656-22-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 64656-22-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 64656-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,6,5 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64656-22:
(7*6)+(6*4)+(5*6)+(4*5)+(3*6)+(2*2)+(1*2)=140
140 % 10 = 0
So 64656-22-0 is a valid CAS Registry Number.

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64656-22-0Relevant academic research and scientific papers

ASYMMETRICALLY SUBSTITUTED MYOINOSITOL DERIVATIVES. XXXI. THE RESOLUTION OF RACEMIC 1(3),2,4(6),5,6(4)-PENTA-O-BENZYL-sn-MYOINOSITOL THROUGH DIASTEREOMERIC GLYCOSIDES

Sibrikov, Yu. I.,Stepanov, A. E.,Shvets, V. I.

, p. 891 - 896 (2007/10/02)

The racemic pentabenzyl ether of myoinositol was separated into the optical antipodes through the formation and separation of diastereomeric glycosides, followed by isolation of the enantiomers by acid hydrolysis.A comparative study was made of the charac

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