Cas 297747-10-5,1,3,4,5-tetra-O-benzyl-6-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-D-myo-inositol

297747-10-5

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Basic information

Product Name: 1,3,4,5-tetra-O-benzyl-6-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-D-myo-inositol
Synonyms: 1,3,4,5-tetra-O-benzyl-6-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-D-myo-inositol
CAS NO:297747-10-5
Molecular Formula:
Molecular Weight: 1077.28
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: 1,3,4,5-tetra-O-benzyl-6-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-D-myo-inositol(CAS DataBase Reference)
NIST Chemistry Reference: 1,3,4,5-tetra-O-benzyl-6-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-D-myo-inositol(297747-10-5)
EPA Substance Registry System: 1,3,4,5-tetra-O-benzyl-6-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-D-myo-inositol(297747-10-5)

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: 297747-10-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 297747-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,7,7,4 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 297747-10:
(8*2)+(7*9)+(6*7)+(5*7)+(4*4)+(3*7)+(2*1)+(1*0)=195
195 % 10 = 5
So 297747-10-5 is a valid CAS Registry Number.

297747-10-5Upstream product

297747-10-5Downstream Products

297747-10-5Relevant academic research and scientific papers

Targeted glycosyl donor delivery for site-selective glycosylation.

Anilkumar,Nair,Fraser-Reid

, p. 2587 - 2589 (2000)

[reaction: see text]n-Pentenyl ortho esters (NPOEs) and n-pentenyl glycosides (NPGs) are interconvertible glycosyl donors which are activated by reaction with halonium ions. In a series of cyclic syn-1,3-diols, NPOEs have been found to specifically glycos

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