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5-(4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1038398-68-3

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1038398-68-3 Usage

Chemical compound

5-(4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carboxylic acid

Class

Pyrazole carboxylic acids

Structure

Pyrazole ring with a carboxylic acid group at the 3-position and a trifluoromethylphenyl group at the 5-position

Potential applications

Medicinal chemistry, drug development, synthesis of pharmaceuticals and agrochemicals

Use

Building block in the synthesis of various compounds

Properties

Ability to modulate biological pathways, interact with specific targets in the body, valuable tool for research in organic chemistry and chemical biology.

Check Digit Verification of cas no

The CAS Registry Mumber 1038398-68-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,8,3,9 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1038398-68:
(9*1)+(8*0)+(7*3)+(6*8)+(5*3)+(4*9)+(3*8)+(2*6)+(1*8)=173
173 % 10 = 3
So 1038398-68-3 is a valid CAS Registry Number.

1038398-68-3Relevant academic research and scientific papers

Design, synthesis, biological evaluation and in silico studies of pyrazole‐based nh2‐acyl oseltamivir analogues as potent neuraminidase inhibitors

Ye, Jiqing,Lin, Lin,Xu, Jinyi,Chan, Paul Kay-Sheung,Yang, Xiao,Ma, Cong

, (2021/05/05)

Oseltamivir represents one of the most successful neuraminidase (NA) inhibitors in the current anti‐influenza therapy. The 150‐cavity of NA was identified as an additional binding pocket, and novel NA inhibitors have been designed to occupy the 150‐cavity

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