Cas 882680-79-7,2-azido-2-deoxy-3,4,6-tri-O-benzyl-D-glucopyranosyl-α-(1->3)-2-methoxymethyl-1,4,5,6-tetra-O-benzyl-L-chiro-inositol

882680-79-7

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Basic information

Product Name: 2-azido-2-deoxy-3,4,6-tri-O-benzyl-D-glucopyranosyl-α-(1->3)-2-methoxymethyl-1,4,5,6-tetra-O-benzyl-L-chiro-inositol
Synonyms: 2-azido-2-deoxy-3,4,6-tri-O-benzyl-D-glucopyranosyl-α-(1->3)-2-methoxymethyl-1,4,5,6-tetra-O-benzyl-L-chiro-inositol
CAS NO:882680-79-7
Molecular Formula:
Molecular Weight: 1042.24
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-azido-2-deoxy-3,4,6-tri-O-benzyl-D-glucopyranosyl-α-(1->3)-2-methoxymethyl-1,4,5,6-tetra-O-benzyl-L-chiro-inositol(CAS DataBase Reference)
NIST Chemistry Reference: 2-azido-2-deoxy-3,4,6-tri-O-benzyl-D-glucopyranosyl-α-(1->3)-2-methoxymethyl-1,4,5,6-tetra-O-benzyl-L-chiro-inositol(882680-79-7)
EPA Substance Registry System: 2-azido-2-deoxy-3,4,6-tri-O-benzyl-D-glucopyranosyl-α-(1->3)-2-methoxymethyl-1,4,5,6-tetra-O-benzyl-L-chiro-inositol(882680-79-7)

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: 882680-79-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 882680-79-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,6,8 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 882680-79:
(8*8)+(7*8)+(6*2)+(5*6)+(4*8)+(3*0)+(2*7)+(1*9)=217
217 % 10 = 7
So 882680-79-7 is a valid CAS Registry Number.

882680-79-7Upstream product

882680-79-7Downstream Products

882680-81-1 2-azido-2-deoxy-3,4,6-tri-O-benzyl-D-glucopyranosyl-α-(1->3)-1,4,5,6-tetra-O-benzyl-L-chiro-inositol

882680-79-7Relevant academic research and scientific papers

Phospholipase cleavage of D- and L-chiro-glycosylphosphoinositides asymmetrically incorporated into liposomal membranes

Bonilla, Julia B.,Belen Cid,Contreras, F.-Xabier,Goni, Felix M.,Martin-Lomas, Manuel

, p. 1513 - 1528 (2008/01/27)

The nature of chiro-inositol-containing inositolphosphoglycans (IPGs), reported to be putative insulin mediators, was studied by examination of the substrate specificities of the phosphatidylinositol-specific phospholi-pase C (PI-PLC) and the glycosylphos

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