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4-(2-phenyl-5-trifluoromethyl-2H-pyrazol-3-yl)-phenylamine is a complex organic compound characterized by a phenylamine core, which is a derivative of aniline. The molecule features a pyrazole ring system, which is a five-membered aromatic ring containing two nitrogen atoms. In this specific compound, the pyrazole ring is substituted with a phenyl group at the 2-position and a trifluoromethyl group at the 5-position. The phenylamine group is attached to the 4-position of the phenyl ring, which is part of the pyrazole structure. 4-(2-phenyl-5-trifluoromethyl-2H-pyrazol-3-yl)-phenylamine is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs and agrochemicals. Its unique structure, with the combination of aromatic rings, a heterocyclic pyrazole, and a trifluoromethyl group, contributes to its reactivity and stability, making it an interesting candidate for further chemical exploration and development.

956263-23-3

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956263-23-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 956263-23-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,2,6 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 956263-23:
(8*9)+(7*5)+(6*6)+(5*2)+(4*6)+(3*3)+(2*2)+(1*3)=193
193 % 10 = 3
So 956263-23-3 is a valid CAS Registry Number.

956263-23-3Downstream Products

956263-23-3Relevant academic research and scientific papers

Methanesulfonamide group at position-4 of the C-5-phenyl ring of 1,5-diarylpyrazole affords a potent class of cyclooxygenase-2 (COX-2) inhibitors

Singh, Sunil Kumar,Vobbalareddy, Saibaba,Shivaramakrishna, Samala,Krishnamraju,Rajjak, Shaikh Abdul,Casturi, Seshagiri Rao,Akhila, Vangoori,Rao, Yeleswarapu Koteswar

, p. 1683 - 1688 (2007/10/03)

The effect of methanesulfonamide (MeSO2NH) group on COX-2 inhibitory activity of 1,5-diarylpyrazole is described. While this group being at position-4 of the N1-phenyl ring was found to be ineffective, its installation at position-4

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