3-Bromo-1-(4-fluorophenyl)-1H-pyrazole-5-carboxylic acid
95%
- Product Code: 45108
CAS:
1251249-98-5
Molecular Weight: | 285.0692 g./mol | Molecular Formula: | C₁₀H₆BrFN₂O₂ |
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EC Number: | MDL Number: | MFCD16683349 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in the field of pharmaceutical research and development, particularly as an intermediate in the synthesis of biologically active compounds. Its structure, featuring both bromine and fluorine substituents, makes it a valuable building block for creating molecules with potential therapeutic properties. It is often employed in the design of drugs targeting specific enzymes or receptors, especially in the development of anti-inflammatory, antimicrobial, or anticancer agents. Additionally, its pyrazole core is a common motif in medicinal chemistry, contributing to the optimization of drug candidates for improved efficacy and selectivity. Researchers also utilize it in the study of structure-activity relationships (SAR) to understand how modifications to its framework influence biological activity.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿2,808.00 |
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3-Bromo-1-(4-fluorophenyl)-1H-pyrazole-5-carboxylic acid
This chemical is primarily used in the field of pharmaceutical research and development, particularly as an intermediate in the synthesis of biologically active compounds. Its structure, featuring both bromine and fluorine substituents, makes it a valuable building block for creating molecules with potential therapeutic properties. It is often employed in the design of drugs targeting specific enzymes or receptors, especially in the development of anti-inflammatory, antimicrobial, or anticancer agents. Additionally, its pyrazole core is a common motif in medicinal chemistry, contributing to the optimization of drug candidates for improved efficacy and selectivity. Researchers also utilize it in the study of structure-activity relationships (SAR) to understand how modifications to its framework influence biological activity.
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