5-(4-Bromophenyl)-3-methylisoxazole-4-carboxylic acid
97%
- Product Code: 119767
CAS:
91182-60-4
Molecular Weight: | 282.09 g./mol | Molecular Formula: | C₁₁H₈BrNO₃ |
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EC Number: | MDL Number: | MFCD16447083 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8℃ |
Product Description:
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 synthesis of heterocyclic molecules. Its structure, featuring a bromophenyl group and an isoxazole ring, makes it valuable for constructing more complex molecules with potential therapeutic applications. Researchers often employ it in the design and synthesis of new drug candidates, especially those targeting inflammation, microbial infections, or other diseases. Additionally, it may be used in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of pharmaceutical agents. Its role in medicinal chemistry highlights its importance in advancing drug discovery and development processes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿837.00 |
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0.250 | 10-20 days | ฿1,260.00 |
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1.000 | 10-20 days | ฿3,069.00 |
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5.000 | 10-20 days | ฿9,261.00 |
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5-(4-Bromophenyl)-3-methylisoxazole-4-carboxylic acid
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 synthesis of heterocyclic molecules. Its structure, featuring a bromophenyl group and an isoxazole ring, makes it valuable for constructing more complex molecules with potential therapeutic applications. Researchers often employ it in the design and synthesis of new drug candidates, especially those targeting inflammation, microbial infections, or other diseases. Additionally, it may be used in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of pharmaceutical agents. Its role in medicinal chemistry highlights its importance in advancing drug discovery and development processes.
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