Cas 208463-33-6,Imidazole-1-carbothioic acid O-[(2R,3R,4R,5R)-4-acetylsulfanylmethyl-5-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-tetrahydro-furan-3-yl] ester

208463-33-6

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Product Name: Imidazole-1-carbothioic acid O-[(2R,3R,4R,5R)-4-acetylsulfanylmethyl-5-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-tetrahydro-furan-3-yl] ester
Synonyms:
CAS NO:208463-33-6
Molecular Formula:
Molecular Weight: 788.036
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: Imidazole-1-carbothioic acid O-[(2R,3R,4R,5R)-4-acetylsulfanylmethyl-5-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-tetrahydro-furan-3-yl] ester(CAS DataBase Reference)
NIST Chemistry Reference: Imidazole-1-carbothioic acid O-[(2R,3R,4R,5R)-4-acetylsulfanylmethyl-5-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-tetrahydro-furan-3-yl] ester(208463-33-6)
EPA Substance Registry System: Imidazole-1-carbothioic acid O-[(2R,3R,4R,5R)-4-acetylsulfanylmethyl-5-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-tetrahydro-furan-3-yl] ester(208463-33-6)

Safety Data

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Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 208463-33-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 208463-33-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,4,6 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 208463-33:
(8*2)+(7*0)+(6*8)+(5*4)+(4*6)+(3*3)+(2*3)+(1*3)=126
126 % 10 = 6
So 208463-33-6 is a valid CAS Registry Number.

208463-33-6Upstream product

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208463-33-6Relevant academic research and scientific papers

Functionalization of nucleoside analogs: Regiospecific conversion of 4'- hydroxyl groups to thioesters and deoxygenation of 3'-hydroxyl groups

Huang, Zhen,Benner, Steven A.

, p. 895 - 899 (1998)

Nucleoside analogs 3a-e were conveniently functionalized by regiospecifically converting 4'-hydroxyl groups to thioesters 4a-e (>90% yield) and reducing 3'-hydroxyl groups to give building blocks 2a-e in 85- 90% yields.

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