6453-44-7 Usage
Chemical structure
1H-Pyrazole-3,5-dicarboxylic acid, 1-phenylconsists of a pyrazole ring with two carboxylic acid groups (-COOH) and a phenyl group (-C6H5) attached to the carbon atom.
Molecular weight
247.21 g/mol
Functional groups
Pyrazole ring, carboxylic acid groups, and a phenyl group.
Biological activities
1H-Pyrazole-3,5-dicarboxylic acid, 1-phenylhas been studied for its potential anti-inflammatory and anti-cancer properties.
Use in synthesis
It is often used as a building block for more complex molecules in the synthesis of pharmaceuticals and agrochemicals.
Chelating properties
It has shown potential as a chelating agent for metal ions and has been used in the preparation of coordination compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 6453-44-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,5 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6453-44:
(6*6)+(5*4)+(4*5)+(3*3)+(2*4)+(1*4)=97
97 % 10 = 7
So 6453-44-7 is a valid CAS Registry Number.
6453-44-7Relevant articles and documents
Preparative scale conversion of D-xylose into hydrophilically functionalized pyrazoles
Diehl, Volker,Cuny, Eckehard,Lichtenthaler, Frieder W.
, p. 1193 - 1201 (2007/10/03)
An expeditious, 4-step procedure is described for the conversion of bulk-scale accessible D-xylose into 5-hydroxymethyl-1-phenylpyrazole-3-carboxaldehyde (3), which, in turn, is converted into various pyrazole building blocks with versatile application profiles, such as the l-phenylpyrazole-3,5-dicarboxylic acid (9), the respective 3,5-dialdehyde (10), and 3,5-bis(aminomethyl)-l-phenylpyrazole(13).
