Cas 16357-48-5,2-thioxo-5-({[3-(trifluoromethyl)phenyl]amino}methylidene)dihydropyrimidine-4,6(1H,5H)-dione

16357-48-5

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Basic information

Product Name: 2-thioxo-5-({[3-(trifluoromethyl)phenyl]amino}methylidene)dihydropyrimidine-4,6(1H,5H)-dione
Synonyms: 2-thioxo-5-({[3-(trifluoromethyl)phenyl]amino}methylidene)dihydropyrimidine-4,6(1H,5H)-dione
CAS NO:16357-48-5
Molecular Formula:
Molecular Weight: 315.276
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: 2-thioxo-5-({[3-(trifluoromethyl)phenyl]amino}methylidene)dihydropyrimidine-4,6(1H,5H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 2-thioxo-5-({[3-(trifluoromethyl)phenyl]amino}methylidene)dihydropyrimidine-4,6(1H,5H)-dione(16357-48-5)
EPA Substance Registry System: 2-thioxo-5-({[3-(trifluoromethyl)phenyl]amino}methylidene)dihydropyrimidine-4,6(1H,5H)-dione(16357-48-5)

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: 16357-48-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 16357-48-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,5 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16357-48:
(7*1)+(6*6)+(5*3)+(4*5)+(3*7)+(2*4)+(1*8)=115
115 % 10 = 5
So 16357-48-5 is a valid CAS Registry Number.

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16357-48-5Relevant academic research and scientific papers

Design and synthesis of new barbituric- and thiobarbituric acid derivatives as potent urease inhibitors: Structure activity relationship and molecular modeling studies

Rauf, Abdul,Shahzad, Sohail,Bajda, Marek,Yar, Muhammad,Ahmed, Faiz,Hussain, Nazar,Akhtar, Muhammad Nadeem,Khan, Ajmal,Jońqczyk, Jakub

, p. 6049 - 6058 (2015)

In this study 36 new compounds were synthesized by condensing barbituric acid or thiobarbituric acid and respective anilines (bearing different substituents) in the presence of triethyl orthoformate in good yields. In vitro urease inhibition studies again

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