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1H-Pyrazole-4-carboxylic acid, 1,3-dimethyl-5-phenyl-, ethyl ester is a chemical compound characterized by the molecular formula C15H16N2O2. It is an ethyl ester derivative of 1H-pyrazole-4-carboxylic acid, featuring two methyl groups and a phenyl group attached to its structure. 1H-Pyrazole-4-carboxylic acid, 1,3-dimethyl-5-phenyl-, ethyl ester is widely recognized in the fields of medicinal chemistry and drug discovery for its role as a building block in the synthesis of diverse pharmaceutical compounds. Additionally, it serves as a key intermediate in the production of specific agrochemicals and specialty chemicals, garnering interest among researchers for its potential biological activities and therapeutic applications.

77435-42-8

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77435-42-8 Usage

Uses

Used in Medicinal Chemistry and Drug Discovery:
1H-Pyrazole-4-carboxylic acid, 1,3-dimethyl-5-phenyl-, ethyl ester is utilized as a building block for the synthesis of various pharmaceutical compounds. Its unique structure and functional groups make it a valuable component in the development of new drugs with potential therapeutic benefits.
Used in Agrochemicals Production:
1H-Pyrazole-4-carboxylic acid, 1,3-dimethyl-5-phenyl-, ethyl ester also serves as a key intermediate in the production of certain agrochemicals, contributing to the development of effective solutions for agricultural applications.
Used in Specialty Chemicals Production:
1H-Pyrazole-4-carboxylic acid, 1,3-dimethyl-5-phenyl-, ethyl ester is employed in the synthesis of specialty chemicals, where its specific properties can be leveraged to create high-value products for various industries.
Used in Research and Development:
Due to its potential biological activities, 1H-Pyrazole-4-carboxylic acid, 1,3-dimethyl-5-phenyl-, ethyl ester is of interest to researchers who are exploring its possible therapeutic applications and furthering the understanding of its properties and interactions within biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 77435-42-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,3 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77435-42:
(7*7)+(6*7)+(5*4)+(4*3)+(3*5)+(2*4)+(1*2)=148
148 % 10 = 8
So 77435-42-8 is a valid CAS Registry Number.

77435-42-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1,3-dimethyl-5-phenylpyrazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names 1H-Pyrazole-4-carboxylic acid,1,3-dimethyl-5-phenyl-,ethyl ester

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:77435-42-8 SDS

77435-42-8Relevant academic research and scientific papers

CALPAIN MODULATORS AND THERAPEUTIC USES THEREOF

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, (2018/04/17)

Disclosed herein are small molecule calpain modulator compositions, pharmaceutical compositions, the use and preparation thereof.

PYRAZOLE DERIVATIVES AS PHOSPHOINOSITIDE 3-KINASES INHIBITORS

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Paragraph 0133; 0134; 0135; 0136, (2017/09/02)

Compounds of formula (I) defined herein are phosphoinositide 3-kinases (PI3K) inhibitors and are useful for the treatment of disorders associated with PI3K enzymes.

Decarboxylative Fluorination of Electron-Rich Heteroaromatic Carboxylic Acids with Selectfluor

Yuan, Xi,Yao, Jian-Fei,Tang, Zhen-Yu

, p. 1410 - 1413 (2017/03/23)

A transition-metal-free decarboxylative fluorination of electron-rich five-membered heteroaromatics, including furan-, pyrazole-, isoxazole-, thiophene-, indole-, benzofuran- and indazolecarboxylic acids, with Selectfluor is reported. Fluorinated dimer products were observed for nitrogen-containing heteroaromatic carboxylic acids, such as indole and pyrazole. An effective method has been developed to synthesize the monomer of 2- and 3-fluoroindoles with Li2CO3 as base at low temperature.

Synthesis of 4-Acyl- and 4-Alkoxy-carbonylpyrazoles

Al-Saleh, Fowzia S.,Khawaja, Ibtisam K. Al,Joule, John A.

, p. 642 - 645 (2007/10/02)

N'-Aroyl- or N'-acetyl, N'-phenyl- or N'-methyl-hydrazino-derivatives (1) of 1,3-dicarbonyl compounds can be converted by mild base treatment into 5-aryl- or 5-methyl-, 1-phenyl- or 1-methylpyrazoles carrying an acyl or alkoxycarbonyl group at C-4.

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