2-[(Boc-amino)methyl]-5-bromothiophene
96%
- Product Code: 64938
CAS:
215183-27-0
| Molecular Weight: | 292.19 g./mol | Molecular Formula: | C₁₀H₁₄BrNO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03659715 | |
| Melting Point: | 48-53 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs), especially those targeting therapeutic areas such as oncology and neurology. The Boc (tert-butoxycarbonyl) protecting group in the molecule allows for selective reactions, making it valuable in multi-step synthetic processes. Additionally, its bromothiophene moiety is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to construct more complex structures. This compound is also used in the development of materials for organic electronics, where thiophene derivatives are known for their conductive properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,691.00 |
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| 1.000 | 10-20 days | ฿7,191.00 |
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| 5.000 | 10-20 days | ฿26,991.00 |
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2-[(Boc-amino)methyl]-5-bromothiophene
This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs), especially those targeting therapeutic areas such as oncology and neurology. The Boc (tert-butoxycarbonyl) protecting group in the molecule allows for selective reactions, making it valuable in multi-step synthetic processes. Additionally, its bromothiophene moiety is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to construct more complex structures. This compound is also used in the development of materials for organic electronics, where thiophene derivatives are known for their conductive properties.
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