Cas 91021-92-0,3-(2'-deoxy-β-D-erythro-pentofuranosyl)-6-hydroxy-5,6,7,8-tetrahydropyrimido[1,2-a]purine-10(3H)-one

91021-92-0

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Basic information

Product Name: 3-(2'-deoxy-β-D-erythro-pentofuranosyl)-6-hydroxy-5,6,7,8-tetrahydropyrimido[1,2-a]purine-10(3H)-one
Synonyms: 3-(2'-deoxy-β-D-erythro-pentofuranosyl)-6-hydroxy-5,6,7,8-tetrahydropyrimido[1,2-a]purine-10(3H)-one
CAS NO:91021-92-0
Molecular Formula:
Molecular Weight: 323.308
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: 3-(2'-deoxy-β-D-erythro-pentofuranosyl)-6-hydroxy-5,6,7,8-tetrahydropyrimido[1,2-a]purine-10(3H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-(2'-deoxy-β-D-erythro-pentofuranosyl)-6-hydroxy-5,6,7,8-tetrahydropyrimido[1,2-a]purine-10(3H)-one(91021-92-0)
EPA Substance Registry System: 3-(2'-deoxy-β-D-erythro-pentofuranosyl)-6-hydroxy-5,6,7,8-tetrahydropyrimido[1,2-a]purine-10(3H)-one(91021-92-0)

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: 91021-92-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 91021-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,2 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 91021-92:
(7*9)+(6*1)+(5*0)+(4*2)+(3*1)+(2*9)+(1*2)=100
100 % 10 = 0
So 91021-92-0 is a valid CAS Registry Number.

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91021-92-0Relevant academic research and scientific papers

An ammonium bicarbonate-enhanced stable isotope dilution UHPLC-MS/MS method for sensitive and accurate quantification of acrolein-DNA adducts in human leukocytes

Yin, Ruichuan,Liu, Shengquan,Zhao, Chao,Lu, Meiling,Tang, Moon-Shong,Wang, Hailin

, p. 3190 - 3197 (2013)

Acrolein (Acr), a ubiquitous environmental pollutant, can react directly with genomic DNA to form mutagenic adducts without undergoing metabolic activation. To sensitively and accurately quantify Acr-DNA adducts (including structural isomers and stereoiso

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