Cas 157364-88-0,Acetic acid (2S,3R,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-((E)-1-methyl-propenyloxy)-tetrahydro-pyran-3-yl ester

157364-88-0

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Basic information

Product Name: Acetic acid (2S,3R,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-((E)-1-methyl-propenyloxy)-tetrahydro-pyran-3-yl ester
Synonyms: Acetic acid (2S,3R,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-((E)-1-methyl-propenyloxy)-tetrahydro-pyran-3-yl ester
CAS NO:157364-88-0
Molecular Formula:
Molecular Weight: 546.661
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: Acetic acid (2S,3R,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-((E)-1-methyl-propenyloxy)-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2S,3R,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-((E)-1-methyl-propenyloxy)-tetrahydro-pyran-3-yl ester(157364-88-0)
EPA Substance Registry System: Acetic acid (2S,3R,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-((E)-1-methyl-propenyloxy)-tetrahydro-pyran-3-yl ester(157364-88-0)

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: 157364-88-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 157364-88-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,3,6 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 157364-88:
(8*1)+(7*5)+(6*7)+(5*3)+(4*6)+(3*4)+(2*8)+(1*8)=160
160 % 10 = 0
So 157364-88-0 is a valid CAS Registry Number.

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157364-88-0Relevant academic research and scientific papers

vinyl Glycosides in Oligosaccharide Synthesis (Part 1): A New Latent-Active Glycosylation Strategy.

Boons, Geert-Jan,Isles, Stephen

, p. 3593 - 3596 (1994)

We have developed a novel latent-active glycosylation strategy.This glycosylation strategy is based on isomerisation of substituted allyl glycosides to give vinyl glycosides which can subsequently be used in a Lewis acid mediated glycosylation reaction.Th

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