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Phenylpyruvic acid 2,4-dinitrophenylhydrazone is a chemical compound derived from phenylpyruvic acid, which is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound is formed by the reaction of phenylpyruvic acid with 2,4-dinitrophenylhydrazine, resulting in a hydrazone derivative. This derivative is often used in analytical chemistry as a derivative for the detection and quantification of phenylpyruvic acid, due to its distinct UV-Vis absorption properties. The compound has a molecular formula of C15H12N4O5 and a molecular weight of 324.28 g/mol. It is a yellow crystalline solid, soluble in organic solvents, and is used in various applications, including the diagnosis of phenylketonuria, a genetic disorder characterized by the buildup of phenylpyruvic acid in the blood.

7662-37-5

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7662-37-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7662-37-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,6 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7662-37:
(6*7)+(5*6)+(4*6)+(3*2)+(2*3)+(1*7)=115
115 % 10 = 5
So 7662-37-5 is a valid CAS Registry Number.

7662-37-5Downstream Products

7662-37-5Relevant academic research and scientific papers

The photochemistry of N-p-toluenesulfonyl peptides: The peptide bond as an electron donor

Hill, Roger R.,Moore, Sharon A.,Roberts, David R.

, p. 1439 - 1446 (2005)

The scope of photobiological processes that involve absorbers within a protein matrix may be limited by the vulnerability of the peptide group to attack by highly reactive redox centers consequent upon electronic excitation. We have explored the nature of this vulnerability by undertaking comprehensive product analyses of aqueous photolysates of 12 N-p-toluene-sulfonyl peptides with systematically selected structures. The results indicate that degradation includes a major pathway that is initiated by intramolecular electron transfer in which the peptide bond serves as electron donor, and the data support the likelihood' of a relay process in dipeptide derivatives.

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