1-(3,5-Dichlorophenyl)-5-propyl-1H-pyrazole-4-carboxylic acid

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Reagent Code: #169115
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CAS Number 306936-60-7

science Other reagents with same CAS 306936-60-7

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Weight 299.15 g/mol
Formula C₁₃H₁₂Cl₂N₂O₂
badge Registry Numbers
MDL Number MFCD02677727
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Storage Room temperature

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Used primarily as a key intermediate in the synthesis of pyrazole-based pharmaceuticals and agrochemicals. Its structure supports the development of compounds with biological activity, particularly in fungicides and herbicides. The carboxylic acid group allows for easy derivatization, enabling the formation of amides, esters, or salts that enhance bioavailability or target specificity. Commonly employed in research settings for designing new active ingredients in crop protection agents due to the electron-withdrawing chloro-substituents that improve stability and binding affinity. Also explored in medicinal chemistry for potential anti-inflammatory or antimicrobial agents.

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inventory 1g
10-20 days ฿10,540.00

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1-(3,5-Dichlorophenyl)-5-propyl-1H-pyrazole-4-carboxylic acid
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Used primarily as a key intermediate in the synthesis of pyrazole-based pharmaceuticals and agrochemicals. Its structure supports the development of compounds with biological activity, particularly in fungicides and herbicides. The carboxylic acid group allows for easy derivatization, enabling the formation of amides, esters, or salts that enhance bioavailability or target specificity. Commonly employed in research settings for designing new active ingredients in crop protection agents due to the electro

Used primarily as a key intermediate in the synthesis of pyrazole-based pharmaceuticals and agrochemicals. Its structure supports the development of compounds with biological activity, particularly in fungicides and herbicides. The carboxylic acid group allows for easy derivatization, enabling the formation of amides, esters, or salts that enhance bioavailability or target specificity. Commonly employed in research settings for designing new active ingredients in crop protection agents due to the electron-withdrawing chloro-substituents that improve stability and binding affinity. Also explored in medicinal chemistry for potential anti-inflammatory or antimicrobial agents.

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