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1,3,5-Triphenylbarbituric acid is a white crystalline compound with the chemical formula C25H18N2O3. It is a derivative of barbituric acid, where three phenyl groups are attached to the carbon atoms at positions 1, 3, and 5. This organic compound is known for its strong fluorescence properties, making it useful as a fluorescent probe in analytical chemistry. It is also employed as a reagent in various chemical reactions and as a ligand in coordination chemistry. Due to its unique structure and properties, 1,3,5-triphenylbarbituric acid has potential applications in the development of new materials and the study of molecular interactions.

5167-31-7

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5167-31-7 Usage

Classification

Barbiturate derivative

Function

Potent inhibitor of inosine monophosphate dehydrogenase

Treatment of cancer

Inhibits growth of various cancer cell lines

Neuroprotective properties

Investigated for potential use in treating neurodegenerative diseases

Ongoing research

Exploring medicinal applications and further understanding of its properties and effects

Check Digit Verification of cas no

The CAS Registry Mumber 5167-31-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,6 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5167-31:
(6*5)+(5*1)+(4*6)+(3*7)+(2*3)+(1*1)=87
87 % 10 = 7
So 5167-31-7 is a valid CAS Registry Number.
InChI:InChI=1/C22H16N2O3/c25-20-19(16-10-4-1-5-11-16)21(26)24(18-14-8-3-9-15-18)22(27)23(20)17-12-6-2-7-13-17/h1-15,19H

5167-31-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-triphenyl-1,3-diazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names Barbituric acid,1,3,5-triphenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5167-31-7 SDS

5167-31-7Relevant academic research and scientific papers

Oxidative Hydroxylation of Heterocyclic β-Dicarbonyl Compounds

Stadlbauer, Wolfgang,Kappe, Thomas

, p. 1005 - 1016 (2007/10/02)

3-Substituted 4-hydroxy-2-quinolones (1), 5-substituted barbituric acids (3) and 4-substituted pyrazolidine-2,4-diones were oxidized to yield the corresponding hydroxyderivatives 2,4 or 9, respectively. - Keywords: 5-Hydroxy-2,4,6-pyrimidine-triones; 4-Hy

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