Cas 496812-02-3,ethyl 2-O-benzoyl-3,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-1-thio-α-D-mannopyranoside

496812-02-3

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Basic information

Product Name: ethyl 2-O-benzoyl-3,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-1-thio-α-D-mannopyranoside
Synonyms: ethyl 2-O-benzoyl-3,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-1-thio-α-D-mannopyranoside
CAS NO:496812-02-3
Molecular Formula:
Molecular Weight: 622.898
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: ethyl 2-O-benzoyl-3,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-1-thio-α-D-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2-O-benzoyl-3,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-1-thio-α-D-mannopyranoside(496812-02-3)
EPA Substance Registry System: ethyl 2-O-benzoyl-3,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-1-thio-α-D-mannopyranoside(496812-02-3)

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: 496812-02-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 496812-02-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,6,8,1 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 496812-02:
(8*4)+(7*9)+(6*6)+(5*8)+(4*1)+(3*2)+(2*0)+(1*2)=183
183 % 10 = 3
So 496812-02-3 is a valid CAS Registry Number.

496812-02-3Upstream product

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496812-02-3Relevant academic research and scientific papers

Synthesis of a polyphosphorylated GPI-anchor core structure

Lahmann, Martina,Garegg, Per J.,Konradsson, Peter,Oscarson, Stefan

, p. 1105 - 1111 (2002)

Using a linear assembly approach a highly differentially protected derivative of the common GPI-anchor core structure (α-D-Man-(1→6)-α-D-Man-(1→2)-α-D-Man-(1→4)- α-D-GlcNH2-(1→6)-D-myo-inositol) has been synthesized. All mannose donors were pre

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