Cas 1344113-75-2,6-[(2-hydroxyphenyl)carbonyl]-5-(4-nitrophenyl)-5,8-dihydropyrido[2,3-d]pyrimidine-2,4,7(1H,3H,6H)-trione

1344113-75-2

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Basic information

Product Name: 6-[(2-hydroxyphenyl)carbonyl]-5-(4-nitrophenyl)-5,8-dihydropyrido[2,3-d]pyrimidine-2,4,7(1H,3H,6H)-trione
Synonyms:
CAS NO:1344113-75-2
Molecular Formula:
Molecular Weight: 422.354
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: 6-[(2-hydroxyphenyl)carbonyl]-5-(4-nitrophenyl)-5,8-dihydropyrido[2,3-d]pyrimidine-2,4,7(1H,3H,6H)-trione(CAS DataBase Reference)
NIST Chemistry Reference: 6-[(2-hydroxyphenyl)carbonyl]-5-(4-nitrophenyl)-5,8-dihydropyrido[2,3-d]pyrimidine-2,4,7(1H,3H,6H)-trione(1344113-75-2)
EPA Substance Registry System: 6-[(2-hydroxyphenyl)carbonyl]-5-(4-nitrophenyl)-5,8-dihydropyrido[2,3-d]pyrimidine-2,4,7(1H,3H,6H)-trione(1344113-75-2)

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: 1344113-75-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1344113-75-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,4,1,1 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1344113-75:
(9*1)+(8*3)+(7*4)+(6*4)+(5*1)+(4*1)+(3*3)+(2*7)+(1*5)=122
122 % 10 = 2
So 1344113-75-2 is a valid CAS Registry Number.

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1344113-75-2Relevant academic research and scientific papers

One-pot chemoselective synthesis of novel fused pyrimidine derivatives

Heravi,Saeedi,Beheshtiha,Oskooie

, p. 737 - 744 (2011)

One-pot triple-component reaction of 4-hydroxycoumarin with aromatic aldehydes and 2-aminobenzimidazole, 3-amino-1H-1,2,4-triazole, or 6-aminouracil in acetonitrile in the presence of catalytic amounts of sulfamic acid led to a chemoselective synthesis of

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