4-(4-Bromo-2-fluorophenylsulfonyl)piperazine-1-carboxylic acid tert-butyl ester
95%
- Product Code: 90423
CAS:
937014-34-1
| Molecular Weight: | 423.3 g./mol | Molecular Formula: | C₁₅H₂₀BrFN₂O₄S |
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| EC Number: | MDL Number: | MFCD32206479 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the preparation of compounds targeting various therapeutic areas, including central nervous system disorders and cancer. Its structure, featuring a piperazine ring and a sulfonyl group, makes it a versatile building block for designing inhibitors or modulators of specific enzymes or receptors. Researchers often employ it in medicinal chemistry to optimize drug candidates for improved efficacy, selectivity, and pharmacokinetic properties. Additionally, its bromo and fluoro substituents enhance its reactivity in cross-coupling reactions, enabling the creation of complex molecular architectures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿9,270.00 |
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| 0.250 | 10-20 days | ฿37,080.00 |
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4-(4-Bromo-2-fluorophenylsulfonyl)piperazine-1-carboxylic acid tert-butyl ester
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the preparation of compounds targeting various therapeutic areas, including central nervous system disorders and cancer. Its structure, featuring a piperazine ring and a sulfonyl group, makes it a versatile building block for designing inhibitors or modulators of specific enzymes or receptors. Researchers often employ it in medicinal chemistry to optimize drug candidates for improved efficacy, selectivity, and pharmacokinetic properties. Additionally, its bromo and fluoro substituents enhance its reactivity in cross-coupling reactions, enabling the creation of complex molecular architectures.
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