Cas 654075-08-8,9-[5',6'-dideoxy-6'-(dibenzyloxyphosphinyl)-β-D-ribohexofuranosyl]adenine

654075-08-8

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Basic information

Product Name: 9-[5',6'-dideoxy-6'-(dibenzyloxyphosphinyl)-β-D-ribohexofuranosyl]adenine
Synonyms: 9-[5',6'-dideoxy-6'-(dibenzyloxyphosphinyl)-β-D-ribohexofuranosyl]adenine
CAS NO:654075-08-8
Molecular Formula:
Molecular Weight: 525.501
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: 9-[5',6'-dideoxy-6'-(dibenzyloxyphosphinyl)-β-D-ribohexofuranosyl]adenine(CAS DataBase Reference)
NIST Chemistry Reference: 9-[5',6'-dideoxy-6'-(dibenzyloxyphosphinyl)-β-D-ribohexofuranosyl]adenine(654075-08-8)
EPA Substance Registry System: 9-[5',6'-dideoxy-6'-(dibenzyloxyphosphinyl)-β-D-ribohexofuranosyl]adenine(654075-08-8)

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: 654075-08-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 654075-08-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,4,0,7 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 654075-08:
(8*6)+(7*5)+(6*4)+(5*0)+(4*7)+(3*5)+(2*0)+(1*8)=158
158 % 10 = 8
So 654075-08-8 is a valid CAS Registry Number.

654075-08-8Upstream product

654075-07-7 N⁶-benzoyl-9-[5',6'-dideoxy-6'-(dibenzyloxyphosphinyl)-β-D-ribohexofuranosyl]adenine

654075-08-8Downstream Products

654075-08-8Relevant academic research and scientific papers

Design, synthesis, and antiviral activity of adenosine 5′-phosphonate analogues as chain terminators against hepatitis C virus

Koh, Yung-Hyo,Shim, Jae Hoon,Wu, Jim Zhen,Zhong, Weidong,Hong, Zhi,Girardet, Jean-Luc

, p. 2867 - 2875 (2005)

A series of adenosine 5′-phosphonate analogues were designed to mimic naturally occurring adenosine monophosphate. These compounds (1-5) were synthesized and evaluated in a cellular hepatitis C virus (HCV) replication assay. To improve cellular permeabili

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