Cas 952575-80-3,phenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside

952575-80-3

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Basic information

Product Name: phenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside
Synonyms: phenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside
CAS NO:952575-80-3
Molecular Formula:
Molecular Weight: 716.76
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: phenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: phenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside(952575-80-3)
EPA Substance Registry System: phenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzoyl-2-O-levulinoyl-1-thio-β-L-arabinopyranoside(952575-80-3)

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: 952575-80-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 952575-80-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,2,5,7 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 952575-80:
(8*9)+(7*5)+(6*2)+(5*5)+(4*7)+(3*5)+(2*8)+(1*0)=203
203 % 10 = 3
So 952575-80-3 is a valid CAS Registry Number.

952575-80-3Upstream product

952575-80-3Downstream Products

952575-80-3Relevant academic research and scientific papers

A highly convergent chemical synthesis of conformational epitopes of rhamnogalacturonan II

Rao, Yu,Boons, Geert-Jan

, p. 6148 - 6151 (2008/09/17)

(Chemical Equation Presented) Upon careful tuning of the reactivity of glycosyl donors and acceptors, tetra- and hexasaccharide fragments (see structure) of the B chain of rhamnogalacturonan II (RGII) were prepared in a convergent and stereoselective mann

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