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1-(3-CHLOROPHENYL)-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID is a pyrazole derivative chemical compound with a chlorophenyl group, a trifluoromethyl group, and a carboxylic acid functional group. It has potential applications in the pharmaceutical industry and may exhibit a variety of biological activities and therapeutic potential. Its unique structure and functional groups make it a valuable target for further research and development in medicinal chemistry.

98534-82-8

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98534-82-8 Usage

Uses

Used in Pharmaceutical Industry:
1-(3-CHLOROPHENYL)-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID is used as a building block for the synthesis of various drug candidates due to its potential biological activities and therapeutic potential. Its unique structure and functional groups contribute to its value in medicinal chemistry research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 98534-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,5,3 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98534-82:
(7*9)+(6*8)+(5*5)+(4*3)+(3*4)+(2*8)+(1*2)=178
178 % 10 = 8
So 98534-82-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H6ClF3N2O2/c12-6-2-1-3-7(4-6)17-9(11(13,14)15)8(5-16-17)10(18)19/h1-5H,(H,18,19)

98534-82-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-chlorophenyl)-5-(trifluoromethyl)pyrazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-(3-Chlorophenyl)-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:98534-82-8 SDS

98534-82-8Downstream Products

98534-82-8Relevant academic research and scientific papers

Synthesis, Biological Evaluation, and 3D-QSAR Studies of N-(Substituted pyridine-4-yl)-1-(substituted phenyl)-5-trifluoromethyl-1 H-pyrazole-4-carboxamide Derivatives as Potential Succinate Dehydrogenase Inhibitors

Wu, Zhibing,Park, Hyung-Yeon,Xie, Dewen,Yang, Jingxin,Hou, Shuaitao,Shahzad, Nasir,Kim, Chan Kyung,Yang, Song

, p. 1214 - 1223 (2021/02/06)

A series of new fungicides that can inhibit the succinate dehydrogenase (SDH) was classified and named as SDH inhibitors by the Fungicide Resistance Action Committee in 2009. To develop more potential SDH inhibitors, we designed and synthesized a novel se

Pyrazole-amides and sulfonamides as sodium channel modulators

-

Page/Page column 13, (2010/02/10)

Compounds of the present invention modulate PN3 in mammals and are useful in treating pain in mammals.

Pyrazole-amides and sulfonamides as sodium channel modulators

-

Page 14, (2010/02/09)

Compounds of the present invention modulate PN3 in mammals and are useful in treating pain in mammals.

Synthesis of 1-Aryl-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic Acids and Esters

Beck, James R.,Wright, Fred L.

, p. 739 - 740 (2007/10/02)

Ethyl 1-aryl-5-(trifluoromethyl)-1H-pyrazole-4-carboxylates 2 were prepared by the condensation of arylhydrazines with ethyl 3-ethoxy-2-(trifluoroacetyl)-2-propenoate (1a) at low temperature.The corresponding acids were also synthesized.X-ray diffraction analysis of an amide derivative 4 verified the position of the trifluoromethyl group on the pyrazole ring.

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