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ETHYL 1-(4-METHOXYPHENYL)-3-METHYL-1H-PYRAZOLE-5-CARBOXYLATE is a pyrazole derivative with the molecular formula C14H16N2O3, featuring an ethyl ester group and a carboxylate group. It is a chemical compound of interest in the fields of organic synthesis and medicinal chemistry, serving as a building block for the development of pharmaceuticals and other bioactive compounds.

218632-36-1

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218632-36-1 Usage

Uses

Used in Pharmaceutical Development:
ETHYL 1-(4-METHOXYPHENYL)-3-METHYL-1H-PYRAZOLE-5-CARBOXYLATE is used as a key intermediate in the synthesis of various pharmaceuticals for the treatment of different diseases and medical conditions. Its unique structure and properties make it a valuable component in drug discovery and development processes.
Used in Organic Synthesis:
In the field of organic synthesis, ETHYL 1-(4-METHOXYPHENYL)-3-METHYL-1H-PYRAZOLE-5-CARBOXYLATE is used as a versatile building block for the creation of complex organic molecules. Its reactivity and functional groups allow for a wide range of chemical reactions, facilitating the synthesis of novel compounds with potential applications in various industries.
Used in Medicinal Chemistry Research:
ETHYL 1-(4-METHOXYPHENYL)-3-METHYL-1H-PYRAZOLE-5-CARBOXYLATE is utilized in medicinal chemistry research to explore its potential as a therapeutic agent or as a structural component in the design of new drugs. Its unique properties and structure make it an attractive candidate for the development of innovative pharmaceuticals.
Used in Drug Discovery:
In the drug discovery process, ETHYL 1-(4-METHOXYPHENYL)-3-METHYL-1H-PYRAZOLE-5-CARBOXYLATE is employed as a starting material or a modifying agent to create new drug candidates. Its chemical properties and structural features contribute to the development of compounds with improved pharmacological profiles and therapeutic potential.
Used in Bioactive Compound Development:
ETHYL 1-(4-METHOXYPHENYL)-3-METHYL-1H-PYRAZOLE-5-CARBOXYLATE is used as a precursor in the development of bioactive compounds with potential applications in various industries, such as agriculture, cosmetics, and pharmaceuticals. Its versatility and reactivity enable the synthesis of a diverse range of bioactive molecules with specific biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 218632-36-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,8,6,3 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 218632-36:
(8*2)+(7*1)+(6*8)+(5*6)+(4*3)+(3*2)+(2*3)+(1*6)=131
131 % 10 = 1
So 218632-36-1 is a valid CAS Registry Number.

218632-36-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(4-methoxyphenyl)-5-methylpyrazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 1-(4-METHOXYPHENYL)-3-METHYL-1H-PYRAZOLE-5-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:218632-36-1 SDS

218632-36-1Relevant articles and documents

PYRAZOLOPYRIDAZINE DERIVATIVES, PREPARATION METHOD THEREOF AND COMPOSITION FOR PREVENTING OR TREATING CANCER COMPRISING THE SAME

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Paragraph 0203-0204; 0209-0212, (2020/11/14)

The present invention is a pyrazolopyridazine derivative. A pharmaceutical composition for preventing or treating cancer contains the pyrazolopyridazin derivative compound Hsp90 according to the present invention as an active ingredient, which can be used as Hsp90 a pharmaceutical composition for preventing or treating Hsp90-related diseases such as melanoma, brain tumor, breast cancer, lung cancer and the like. (by machine translation)

Design and Synthesis of Imidazole and Triazole Pyrazoles as Mycobacterium Tuberculosis CYP121A1 Inhibitors

Kishk, Safaa M.,McLean, Kirsty J.,Sood, Sakshi,Smith, Darren,Evans, Jack W.D.,Helal, Mohamed A.,Gomaa, Mohamed S.,Salama, Ismail,Mostafa, Samia M.,de Carvalho, Luiz Pedro S.,Levy, Colin W.,Munro, Andrew W.,Simons, Claire

, p. 995 - 1011 (2019/08/06)

The emergence of untreatable drug-resistant strains of Mycobacterium tuberculosis is a major public health problem worldwide, and the identification of new efficient treatments is urgently needed. Mycobacterium tuberculosis cytochrome P450 CYP121A1 is a p

Microwave-assisted synthesis of tetrazolyl pyrazole amides

Hu, Jun,Wang, Jikui,Zhou, Taoyu,Xu, Yanhua

experimental part, p. 525 - 527 (2011/11/30)

A rapid and efficient microwave-assisted synthesis N-(1H-tetrazol-5-yl) derivatives of 3-methyl-1-phenyl-1H-pyrazole- 5-carboxamide is described. These tetrazole pyrazole amides have interesting bacteriocidal, pesticidal, herbicidal and antimicrobial activities. They were identified by IR and 1H NMR elemental analyses. The target compounds were obtained in a shorter reaction time compared to conventional heating methods.

Pyrazoles for the treatment of obesity and other CNS disorders

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Page/Page column 14; 15; 26; 27, (2010/11/28)

This invention relates to compounds having pharmacological activity, to compositions containing these compounds, and to a method of treatment employing the compounds and compositions. More particularly, this invention concerns certain pyrazole derivatives, their salts and solvates. These compounds have H3 histamine receptor binding activity. This invention also relates to pharmaceutical compositions containing these compounds and to a method of treating disorders in which histamine H3 receptor modulation is beneficial.

Discovery of 1-(2-Aminomethylphenyl)-3-trifluoromethyl-N-[3-fluoro-2′ -(aminosulfonyl)[1,1′-biphenyl)]-4-yl]-1H-pyrazole-5-carboxyamide (DPC602), a Potent, Selective, and Orally Bioavailable Factor Xa Inhibitor

Pruitt, James R.,Pinto, Donald J. P.,Galemmo Jr., Robert A.,Alexander, Richard S.,Rossi, Karen A.,Wells, Brian L.,Drummond, Spencer,Bostrom, Lori L.,Burdick, Debra,Bruckner, Robert,Chen, Haiying,Smallwood, Angela,Wong, Pancras C.,Wright, Matthew R.,Bai, Steven,Luettgen, Joseph M.,Knabb, Robert M.,Lam, Patrick Y. S.,Wexler, Ruth R.

, p. 5298 - 5315 (2007/10/03)

Factor Xa, a serine protease, is at the critical juncture between the intrinsic and extrinsic pathways of the coagulation cascade. Inhibition of factor Xa has the potential to provide effective treatment for both venous and arterial thrombosis. We recentl

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