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Ethyl 4-pyridazinecarboxylate, a chemical compound with the molecular formula C8H8N2O2, is a derivative of pyridazine, a six-membered aromatic heterocycle containing two nitrogen atoms. Ethyl 4-pyridazinecarboxylate is recognized for its diverse biological activities, such as antifungal, antibacterial, and anti-inflammatory properties, and serves as a crucial intermediate in the synthesis of pharmaceuticals and agricultural chemicals. It also functions as a building block for developing novel chemical entities with potential therapeutic applications, making it an important chemical intermediate in various industries and pharmaceutical sectors.

39123-39-2

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39123-39-2 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 4-pyridazinecarboxylate is used as a chemical intermediate for the synthesis of various pharmaceuticals, leveraging its biological activities to contribute to the development of new drugs with potential therapeutic applications.
Used in Agricultural Chemical Industry:
In the agricultural sector, Ethyl 4-pyridazinecarboxylate is utilized as an intermediate in the production of agricultural chemicals, taking advantage of its antifungal and antibacterial properties to create compounds that can protect crops and enhance agricultural productivity.
Used in Research and Development:
Ethyl 4-pyridazinecarboxylate is employed as a building block in the research and development of novel chemical entities, providing a foundation for the creation of innovative compounds with potential applications in medicine and other fields.
Used in Drug Synthesis:
As a key component in drug synthesis, Ethyl 4-pyridazinecarboxylate is used to develop new pharmaceuticals that can address various health conditions, capitalizing on its diverse biological properties to enhance the effectiveness and range of available treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 39123-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,2 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 39123-39:
(7*3)+(6*9)+(5*1)+(4*2)+(3*3)+(2*3)+(1*9)=112
112 % 10 = 2
So 39123-39-2 is a valid CAS Registry Number.

39123-39-2SDS

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 Pyridazine-4-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl pyridazine-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:39123-39-2 SDS

39123-39-2Relevant academic research and scientific papers

Novel HIV reverse transcriptase inhibitors

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Page/Page column 107, (2008/06/13)

The invention is related to compounds of Formula (I), (II), or (III): or a pharmaceutically acceptable salt, solvate, ester, and/or phosphonate thereof, compositions containing such compounds, and therapeutic methods that include the administration of such compounds.

MGluR5 modulators I

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Page/Page column 26, (2008/06/13)

The present invention is directed to novel compounds, to a process for their preparation, their use in therapy and pharmaceutical compositions comprising the novel compounds.

PYRIDAZINES XXIV. APPLICATION OF RADICALIC ETHOXYCARBONYLATION TO THE SYNTHESIS OF PYRIDAZINE MONO- AND POLYCARBOXYLIC ACID ESTERS

Heinisch, Gottfried,Loetsch, Gerhard

, p. 1199 - 1206 (2007/10/02)

Reactivity of pyridazines 1, 2, 3, 16 towards ethoxycarbonylradical (generated by redox decomposition of oxyhydroperoxyde of ethylpyruvate) was studied.Application of this type of homolytic substitution for synthesis of hitherto not accessible pyridazine carboxylic acid esters 6, 8, 9, 12, 13, 14, 15, 17 is demonstrated.In addition improved synthesis of diethyl 4,5-pyridazinedicarboxylate (5) is proposed.

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