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ETHYL 1-(4-CHLOROPHENYL)-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLATE is a pyrazole derivative with the molecular formula C14H10ClF3N2O2. It is an organic compound that features a trifluoromethyl group and a chlorophenyl group, contributing to its unique chemical and physical properties. ETHYL 1-(4-CHLOROPHENYL)-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLATE is recognized for its potential biological and pharmacological properties, making it a valuable building block in the synthesis of pharmaceuticals and agrochemicals.

112055-36-4

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112055-36-4 Usage

Uses

Used in Pharmaceutical Synthesis:
ETHYL 1-(4-CHLOROPHENYL)-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLATE is used as an intermediate in the synthesis of various pharmaceuticals for its potential biological and pharmacological properties. Its unique structure, including the electron-withdrawing trifluoromethyl group and the chlorophenyl group, allows for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Synthesis:
In the agrochemical industry, ETHYL 1-(4-CHLOROPHENYL)-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLATE is used as a key building block in the creation of novel agrochemicals. Its chemical properties make it suitable for the development of new pesticides and other agricultural chemicals that can enhance crop protection and yield.
Used in Organic Synthesis:
ETHYL 1-(4-CHLOROPHENYL)-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLATE is utilized as a versatile reagent in organic synthesis. Its unique structure allows for various chemical reactions, enabling the synthesis of a wide range of organic compounds with diverse applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 112055-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,0,5 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112055-36:
(8*1)+(7*1)+(6*2)+(5*0)+(4*5)+(3*5)+(2*3)+(1*6)=74
74 % 10 = 4
So 112055-36-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H4FI/c7-5-2-1-3-6(8)4-5/h1-4H

112055-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2-(4-chlorophenyl)-3-(trifluoromethyl)-pyrazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 1-(4-chlorophenyl)-5-(trifluoromethyl)pyrazole-4-carboxylate

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:112055-36-4 SDS

112055-36-4Relevant 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

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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