3-(4-Bromophenyl)-1-phenyl-1h-pyrazole-4-carboxylic acid

95%

Reagent Code: #124146
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CAS Number 372107-34-1

science Other reagents with same CAS 372107-34-1

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Weight 343.17 g/mol
Formula C₁₆H₁₁BrN₂O₂
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MDL Number MFCD01828977
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This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the design of pyrazole derivatives. These derivatives are often explored for their potential therapeutic applications, including anti-inflammatory, antimicrobial, and anticancer properties. Additionally, it is used in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of drug candidates. Its bromophenyl and carboxylic acid functional groups make it a versatile building block for further chemical modifications in medicinal chemistry.

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inventory 100mg
10-20 days ฿3,861.00

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3-(4-Bromophenyl)-1-phenyl-1h-pyrazole-4-carboxylic acid
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This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the design of pyrazole derivatives. These derivatives are often explored for their potential therapeutic applications, including anti-inflammatory, antimicrobial, and anticancer properties. Additionally, it is used in the study of structure-activity relationships (SAR) to optimize the efficacy and se

This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the design of pyrazole derivatives. These derivatives are often explored for their potential therapeutic applications, including anti-inflammatory, antimicrobial, and anticancer properties. Additionally, it is used in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of drug candidates. Its bromophenyl and carboxylic acid functional groups make it a versatile building block for further chemical modifications in medicinal chemistry.

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