Cas 98750-27-7,2-amino-7-(3',5'-di-O-benzoyl-2'-deoxy-β-D-erythro-pentofuranosyl)-3,4-dihydroimidazo<5,1-f><1,2,4>triazin-4-one

98750-27-7

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Basic information

Product Name: 2-amino-7-(3',5'-di-O-benzoyl-2'-deoxy-β-D-erythro-pentofuranosyl)-3,4-dihydroimidazo<5,1-f><1,2,4>triazin-4-one
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CAS NO:98750-27-7
Molecular Formula:
Molecular Weight: 475.461
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: 2-amino-7-(3',5'-di-O-benzoyl-2'-deoxy-β-D-erythro-pentofuranosyl)-3,4-dihydroimidazo<5,1-f><1,2,4>triazin-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-amino-7-(3',5'-di-O-benzoyl-2'-deoxy-β-D-erythro-pentofuranosyl)-3,4-dihydroimidazo<5,1-f><1,2,4>triazin-4-one(98750-27-7)
EPA Substance Registry System: 2-amino-7-(3',5'-di-O-benzoyl-2'-deoxy-β-D-erythro-pentofuranosyl)-3,4-dihydroimidazo<5,1-f><1,2,4>triazin-4-one(98750-27-7)

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 98750-27-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 98750-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,5 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 98750-27:
(7*9)+(6*8)+(5*7)+(4*5)+(3*0)+(2*2)+(1*7)=177
177 % 10 = 7
So 98750-27-7 is a valid CAS Registry Number.

98750-27-7Upstream product

98750-27-7Downstream Products

98750-27-7Relevant academic research and scientific papers

Synthesis of Imidazo-fused Bridgehead-nitrogen 2'-Deoxyribo-C-nucleosides: Coupling-Elimination Reactions of 2,5-Anhydro-3,4,6-tri-O-benzoyl-D-allonic Acid

Knutsen, Lars J. S.,Judkins, Brian D.,Newton, Roger F.,Scopes, David C.,Graham, Klinkert

, p. 621 - 630 (2007/10/02)

A short synthesis of imidazo-fused bridgehead 2'-deoxyribo-C-nucleosides has been developed.This is based on a coupling-elimination reaction of 2,5-anhydro-3,4,6-tri-O-benzoyl-D-allonic acid with a series of aminoalkyl-substituted heterocycles and alcohol

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