Cas 1190096-24-2,1-(5-benzoyl-2,3-dideoxy-β-D-glyceropent-2-enofuranosyl)pyrazin-2-one

1190096-24-2

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Basic information

Product Name: 1-(5-benzoyl-2,3-dideoxy-β-D-glyceropent-2-enofuranosyl)pyrazin-2-one
Synonyms: 1-(5-benzoyl-2,3-dideoxy-β-D-glyceropent-2-enofuranosyl)pyrazin-2-one
CAS NO:1190096-24-2
Molecular Formula:
Molecular Weight: 298.298
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-(5-benzoyl-2,3-dideoxy-β-D-glyceropent-2-enofuranosyl)pyrazin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-(5-benzoyl-2,3-dideoxy-β-D-glyceropent-2-enofuranosyl)pyrazin-2-one(1190096-24-2)
EPA Substance Registry System: 1-(5-benzoyl-2,3-dideoxy-β-D-glyceropent-2-enofuranosyl)pyrazin-2-one(1190096-24-2)

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: 1190096-24-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1190096-24-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,0,9 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1190096-24:
(9*1)+(8*1)+(7*9)+(6*0)+(5*0)+(4*9)+(3*6)+(2*2)+(1*4)=142
142 % 10 = 2
So 1190096-24-2 is a valid CAS Registry Number.

1190096-24-2Upstream product

1190096-21-9 1-(5-O-benzoyl-2,3-bis-O-((methylthio)thiocarbonyl)-β-D-ribofuranosyl)pyrazin-2-one

1190096-24-2Downstream Products

1190096-24-2Relevant academic research and scientific papers

3-Substituted pyrazinone nucleosidesA new family of D4T analogues

Batoux, Nathalie,Granet, Robert,Zerrouki, Rachida,Krausz, Pierre

experimental part, p. 866 - 873 (2010/08/21)

The synthesis of a new family of D4T analogues is described to study the influence of pyrazinone base on antiretroviral power. Substitution of 3H by methyl or n-decyl increases the lipophilic character and may facilitate diffusion across cell membranes. T

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