Cas 1154032-40-2,1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-5-chloro-6-(2,4-dichlorophenoxymethyl)uracil

1154032-40-2

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Basic information

Product Name: 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-5-chloro-6-(2,4-dichlorophenoxymethyl)uracil
Synonyms: 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-5-chloro-6-(2,4-dichlorophenoxymethyl)uracil
CAS NO:1154032-40-2
Molecular Formula:
Molecular Weight: 765.988
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: 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-5-chloro-6-(2,4-dichlorophenoxymethyl)uracil(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-5-chloro-6-(2,4-dichlorophenoxymethyl)uracil(1154032-40-2)
EPA Substance Registry System: 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-5-chloro-6-(2,4-dichlorophenoxymethyl)uracil(1154032-40-2)

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: 1154032-40-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1154032-40-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,4,0,3 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1154032-40:
(9*1)+(8*1)+(7*5)+(6*4)+(5*0)+(4*3)+(3*2)+(2*4)+(1*0)=102
102 % 10 = 2
So 1154032-40-2 is a valid CAS Registry Number.

1154032-40-2Upstream product

6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose

1154032-40-2Downstream Products

1154032-43-5 5-chloro-6-(2,4-dichlorophenoxymethyl)-1-(β-D-ribofuranosyl)uracil

1154032-40-2Relevant academic research and scientific papers

Synthesis of new cyclic and acyclic 5-halouridine derivatives as potential antiviral agents

Elshehry, Mohamed F.,Balzarini, Jan,Meier, Chris

, p. 841 - 847 (2009)

The synthesis of new cyclic and acyclic nucleoside analogues was achieved by alkylation of 5-halogenated 6-(2,4-dichlo-rophenoxymethyl)pyrimidine-2,4- dione following the Vorbrueggen coupling procedure. Nucleoside analogues of the 1-[(2-hydroxy-ethoxy)met

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