N-Boc-3-Amino-4-iodopyridine
≥98.0%
- Product Code: 113322
CAS:
154048-89-2
| Molecular Weight: | 320.13 g./mol | Molecular Formula: | C₁₀H₁₃IN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04973410 | |
| Melting Point: | Boiling Point: | 313.221°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. It is particularly valuable in the development of drugs targeting neurological disorders, cancer, and infectious diseases. The Boc protecting group allows for selective reactions, enabling the introduction of other functional groups or further modifications. Its iodine substituent makes it a versatile building block for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in creating complex molecular structures. This compound is also employed in the synthesis of heterocyclic compounds, which are widely used in medicinal chemistry for their diverse biological activities.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Light Yellow To Yellow Solid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿460.00 |
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| 0.250 | 10-20 days | ฿790.00 |
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N-Boc-3-Amino-4-iodopyridine
Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. It is particularly valuable in the development of drugs targeting neurological disorders, cancer, and infectious diseases. The Boc protecting group allows for selective reactions, enabling the introduction of other functional groups or further modifications. Its iodine substituent makes it a versatile building block for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in creating complex molecular structures. This compound is also employed in the synthesis of heterocyclic compounds, which are widely used in medicinal chemistry for their diverse biological activities.
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