2-Bromo-5-(N-Boc-piperidin-3-yl)thiophene
95%
- Product Code: 43269
CAS:
1622834-60-9
| Molecular Weight: | 346.2831 g./mol | Molecular Formula: | C₁₄H₂₀BrNO₂S |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 396.5±42.0 °C at 760 mmHg | |
| Density: | 1.360±0.06 g/cm3 | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the construction of complex molecules, especially those targeting therapeutic applications. The Boc (tert-butoxycarbonyl) group provides protection for the piperidine nitrogen during synthetic processes, allowing for selective reactions at other sites of the molecule. Its thiophene moiety is often employed in the design of drug candidates due to its bioisosteric properties, which can enhance binding affinity and metabolic stability. This compound is particularly relevant in the synthesis of small-molecule inhibitors and bioactive compounds for research in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,784.00 |
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| 0.250 | 10-20 days | ฿14,652.00 |
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| 1.000 | 10-20 days | ฿38,592.00 |
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2-Bromo-5-(N-Boc-piperidin-3-yl)thiophene
This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the construction of complex molecules, especially those targeting therapeutic applications. The Boc (tert-butoxycarbonyl) group provides protection for the piperidine nitrogen during synthetic processes, allowing for selective reactions at other sites of the molecule. Its thiophene moiety is often employed in the design of drug candidates due to its bioisosteric properties, which can enhance binding affinity and metabolic stability. This compound is particularly relevant in the synthesis of small-molecule inhibitors and bioactive compounds for research in medicinal chemistry.
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