tert-butyl 4-(4-iodophenyl)tetrahydro-1(2h)-pyrazinecarboxylate
98%
- Product Code: 77212
CAS:
151978-66-4
| Molecular Weight: | 388.20 g./mol | Molecular Formula: | C₁₅H₂₁IN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the synthesis of potential drug candidates. The presence of the iodophenyl group makes it a useful precursor in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for creating carbon-carbon bonds in medicinal chemistry. Additionally, its tert-butyl ester group provides stability and can be deprotected to reveal a free amine, enabling further functionalization. This chemical is often employed in the design and synthesis of compounds targeting neurological disorders or other therapeutic areas.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,260.00 |
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| 1.000 | 10-20 days | ฿3,390.00 |
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tert-butyl 4-(4-iodophenyl)tetrahydro-1(2h)-pyrazinecarboxylate
This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the synthesis of potential drug candidates. The presence of the iodophenyl group makes it a useful precursor in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for creating carbon-carbon bonds in medicinal chemistry. Additionally, its tert-butyl ester group provides stability and can be deprotected to reveal a free amine, enabling further functionalization. This chemical is often employed in the design and synthesis of compounds targeting neurological disorders or other therapeutic areas.
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