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4-Nitro-1-phenyl-1,2-dihydro-pyrazol-3-one is a chemical compound with the molecular formula C10H9N3O3. It is a derivative of pyrazolone, a heterocyclic compound with a pyrazole ring fused to a ketone. This specific compound features a nitro group at the 4-position, a phenyl group at the 1-position, and a hydrogen atom at the 2-position, forming a dihydro structure. It is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. The compound is typically synthesized through various chemical reactions and can be used as an intermediate in the preparation of more complex molecules.

7409-22-5

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7409-22-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7409-22-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7409-22:
(6*7)+(5*4)+(4*0)+(3*9)+(2*2)+(1*2)=95
95 % 10 = 5
So 7409-22-5 is a valid CAS Registry Number.

7409-22-5Relevant academic research and scientific papers

Synthesis and biological evaluation of new phenidone analogues as potential dual cyclooxygenase (COX-1 and COX-2) and human lipoxygenase (5-LOX) inhibitors

Cusan, Claudia,Spalluto, Giampiero,Prato, Maurizio,Adams, Michael,Bodensieck, Antje,Bauer, Rudolf,Tubaro, Aurelia,Bernardi, Paolo,Da Ros, Tatiana

, p. 7 - 13 (2007/10/03)

A new series of potential human 5-LOX inhibitors structurally related to the 1-phenyl-3-pyrazolidinone (phenidone, 2) has been synthesized and the activity against COX-1, COX-2, and human 5-LOX enzymes has been evaluated. In contrast with literature data, we observed that phenidone resulted to be inactive against human 5-LOX, while retains its activity against cyclooxygenases in a micromolar range. The present results suggest that the substitution of the amino function at the 4-position is detrimental in terms of activity toward COX-1 and COX-2, while the presence of a double bond at the 4,5-position does not alter the biological profile against COX. The absence of activity vs. human 5-LOX strongly suggests a re-consideration of phenidone and its analogs as 5-LOX inhibitors in humans.

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