(S)-6-(4-Chlorophenyl)-2-(3-fluorophenyl)-N-(1-hydroxypropan-2-yl)-3-oxo-2,3-dihydropyridazine-4-carboxamide
98%
Reagent
Code: #99235
CAS Number
2162982-11-6
blur_circular Chemical Specifications
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Molecular Information
Weight
401.82 g/mol
Formula
C₂₀H₁₇ClFN₃O₃
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Registry Numbers
MDL Number
MFCD31736303
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Storage & Handling
Density
1.37±0.1 g/cm3(Predicted)
Storage
room temperature
description Product Description
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of biologically active molecules. Its structure is particularly valuable in the development of potential therapeutic agents targeting various diseases. The presence of both chlorophenyl and fluorophenyl groups enhances its ability to interact with specific biological targets, making it useful in the design of inhibitors for enzymes or receptors involved in pathological processes.
In pharmaceutical research, it is often employed in the creation of compounds aimed at modulating inflammatory responses or treating neurological disorders. The hydroxypropan-2-yl moiety contributes to its solubility and bioavailability, which are critical factors in drug development. Researchers also explore its potential in designing drugs with improved metabolic stability and reduced toxicity.
Additionally, this chemical is studied for its role in the development of novel anti-cancer agents, where its structural features may help in targeting specific pathways involved in tumor growth and proliferation. Its application extends to the optimization of lead compounds during the drug discovery process, ensuring enhanced efficacy and selectivity for therapeutic targets.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | white solid |
Purity | 97.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
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(S)-6-(4-Chlorophenyl)-2-(3-fluorophenyl)-N-(1-hydroxypropan-2-yl)-3-oxo-2,3-dihydropyridazine-4-carboxamide
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of biologically active molecules. Its structure is particularly valuable in the development of potential therapeutic agents targeting various diseases. The presence of both chlorophenyl and fluorophenyl groups enhances its ability to interact with specific biological targets, making it useful in the design of inhibitors for enzymes or receptors involved in pathological processes.
In pharmaceutical research, it is often employed in the creation of compounds aimed at modulating inflammatory responses or treating neurological disorders. The hydroxypropan-2-yl moiety contributes to its solubility and bioavailability, which are critical factors in drug development. Researchers also explore its potential in designing drugs with improved metabolic stability and reduced toxicity.
Additionally, this chemical is studied for its role in the development of novel anti-cancer agents, where its structural features may help in targeting specific pathways involved in tumor growth and proliferation. Its application extends to the optimization of lead compounds during the drug discovery process, ensuring enhanced efficacy and selectivity for therapeutic targets.
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