Cas 204331-83-9,Acetic acid (1R,2S,3S,4R)-2,3,4-triacetoxy-1-(tert-butyl-diphenyl-silanyloxymethyl)-5-ethylsulfanyl-5-methoxy-pentyl ester

204331-83-9

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Basic information

Product Name: Acetic acid (1R,2S,3S,4R)-2,3,4-triacetoxy-1-(tert-butyl-diphenyl-silanyloxymethyl)-5-ethylsulfanyl-5-methoxy-pentyl ester
Synonyms:
CAS NO:204331-83-9
Molecular Formula:
Molecular Weight: 662.874
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 (1R,2S,3S,4R)-2,3,4-triacetoxy-1-(tert-butyl-diphenyl-silanyloxymethyl)-5-ethylsulfanyl-5-methoxy-pentyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (1R,2S,3S,4R)-2,3,4-triacetoxy-1-(tert-butyl-diphenyl-silanyloxymethyl)-5-ethylsulfanyl-5-methoxy-pentyl ester(204331-83-9)
EPA Substance Registry System: Acetic acid (1R,2S,3S,4R)-2,3,4-triacetoxy-1-(tert-butyl-diphenyl-silanyloxymethyl)-5-ethylsulfanyl-5-methoxy-pentyl ester(204331-83-9)

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: 204331-83-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 204331-83-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,3,3 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 204331-83:
(8*2)+(7*0)+(6*4)+(5*3)+(4*3)+(3*1)+(2*8)+(1*3)=89
89 % 10 = 9
So 204331-83-9 is a valid CAS Registry Number.

204331-83-9Upstream product

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204331-83-9Relevant academic research and scientific papers

The synthesis of disaccharides terminating in D-septanosyl residues using acyclic intermediates

McAuliffe, Joseph C.,Hindsgaul, Ole

, p. 307 - 309 (1998)

A general method for the construction of disaccharides containing D-septanosyl residues from acyclic intermediates has been developed. The synthesis of an analogue of N-acetyl D-lactosamine with a D-galactoseptanosyl unit has also been accomplished with the aim of determining the behaviour of this compound as a substrate for several glycosyltransferases.

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