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1H-Pyrazole-4-carboxylic acid is a heterocyclic organic compound with the molecular formula C4H4N2O2. It features a pyrazole ring and a carboxylic acid group, making it a versatile chemical with potential applications in pharmaceuticals, agrochemicals, and organic chemistry research.
Used in Pharmaceutical Industry:
1H-Pyrazole-4-carboxylic acid is used as a key intermediate in the synthesis of various bioactive compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
1H-Pyrazole-4-carboxylic acid is used as a building block for the synthesis of agrochemicals, such as pesticides and herbicides, due to its ability to form stable and effective compounds.
Used in Organic Chemistry Research:
1H-Pyrazole-4-carboxylic acid is used as a valuable chemical in organic chemistry research, serving as a starting material for the synthesis of other complex organic compounds and aiding in the advancement of chemical knowledge and innovation.

138907-76-3

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138907-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138907-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,0 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 138907-76:
(8*1)+(7*3)+(6*8)+(5*9)+(4*0)+(3*7)+(2*7)+(1*6)=163
163 % 10 = 3
So 138907-76-3 is a valid CAS Registry Number.

138907-76-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-(4-bromophenyl)pyrazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names 1-(4-Brom-phenyl)-1H-pyrazol-4-carbonsaeure-aethylester

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:138907-76-3 SDS

138907-76-3Relevant academic research and scientific papers

Synthesis of pyrazole-carboxamides and pyrazole-carboxylic acids derivatives: Simple methods to access powerful building blocks

Ferreira, Byanca Silva,Silva, Rafaela Corrêa,Souto, Bernardo Araújo,Dos Santos, Maurício Silva

, p. 335 - 343 (2021/09/07)

Hybrid systems containing pyrazole moiety show a wide spectrum of biological activities. To access novel hybrids with pyrazole ring, in this work we synthesized twenty pyrazole-carboxylic acids and twenty pyrazole-carboxamides, using simple synthetic methods, to be used as building blocks in the development of new structures.

PYRROLIDINE DERIVATIVES AS INHIBITOR OF FIBROBLAST ACTIVATION PROTEIN (FAP) AND PHARMACEUTICAL COMPOSITION INCLUDING THE SAME

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Paragraph 0293; 0297-0299, (2020/11/24)

The FAP inhibitor is represented by the following formula X. The present invention relates to a pyrrolidine derivative or a pharmaceutically acceptable salt thereof. Chem. X.

nBu3P-catalyzed desulfonylative [3 + 2] cycloadditions of allylic carbonates with arylazosulfones to pyrazole derivatives

Zhang, Qi,Meng, Ling-Guo,Wang, Kuai,Wang, Lei

supporting information, p. 872 - 875 (2015/04/21)

Highly efficient nBu3P-catalyzed desulfonylative [3 + 2] cycloadditions of allylic carbonates with arylazosulfones were developed for the synthesis of pyrazole derivatives. The reactions proceed smoothly under mild conditions to gene

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