Cas 848866-41-1,phenyl 2,3,4-tri-O-benzyl-6-O-[2-[(4-phenylbenzyl)oxycarbonyl]benzoyl]-1-thio-α-D-glucopyranoside

848866-41-1

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Basic information

Product Name: phenyl 2,3,4-tri-O-benzyl-6-O-[2-[(4-phenylbenzyl)oxycarbonyl]benzoyl]-1-thio-α-D-glucopyranoside
Synonyms: phenyl 2,3,4-tri-O-benzyl-6-O-[2-[(4-phenylbenzyl)oxycarbonyl]benzoyl]-1-thio-α-D-glucopyranoside
CAS NO:848866-41-1
Molecular Formula:
Molecular Weight: 857.036
EINECS: N/A
Product Categories: N/A
Mol File: 848866-41-1.mol
Article Data: 1

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: phenyl 2,3,4-tri-O-benzyl-6-O-[2-[(4-phenylbenzyl)oxycarbonyl]benzoyl]-1-thio-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: phenyl 2,3,4-tri-O-benzyl-6-O-[2-[(4-phenylbenzyl)oxycarbonyl]benzoyl]-1-thio-α-D-glucopyranoside(848866-41-1)
EPA Substance Registry System: phenyl 2,3,4-tri-O-benzyl-6-O-[2-[(4-phenylbenzyl)oxycarbonyl]benzoyl]-1-thio-α-D-glucopyranoside(848866-41-1)

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: 848866-41-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 848866-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,8,6 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 848866-41:
(8*8)+(7*4)+(6*8)+(5*8)+(4*6)+(3*6)+(2*4)+(1*1)=231
231 % 10 = 1
So 848866-41-1 is a valid CAS Registry Number.

848866-41-1Upstream product

3597-91-9 biphenyl-4-yl methanol

848866-41-1Downstream Products

848866-41-1Relevant articles and documents

Stereoselective glycosylation using the long-range effect of a [2-(4-phenylbenzyl)oxycarbonyl]benzoyl group

Tokimoto, Hiroomi,Fujimoto, Yukari,Fukase, Koichi,Kusumoto, Shoichi

, p. 441 - 447 (2005)

Highly α-selective glucosylation was effected by virtue of the solvent effect of cyclopentyl methyl ether and the long-range assistance of bulky 6-O-protective groups. Higher α-selectivity was obtained by the use of this solvent in comparison to conventio

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