7-chloro-2-iodothieno[3,2-b]pyridine
97%
- Product Code: 54475
CAS:
602303-26-4
| Molecular Weight: | 295.53 g./mol | Molecular Formula: | C₇H₃ClINS |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the development of various pharmaceutical compounds. Its unique structure, featuring both chlorine and iodine substituents on a thienopyridine core, makes it a valuable building block for creating molecules with potential biological activity. Researchers often employ it in the synthesis of heterocyclic compounds that are explored for their therapeutic properties, particularly in areas such as antimicrobial, antiviral, and anticancer drug development. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse chemical libraries for high-throughput screening in drug discovery programs.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Pale-yellow to Yellow-brown solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,950.00 |
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| 1.000 | 10-20 days | ฿9,520.00 |
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7-chloro-2-iodothieno[3,2-b]pyridine
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the development of various pharmaceutical compounds. Its unique structure, featuring both chlorine and iodine substituents on a thienopyridine core, makes it a valuable building block for creating molecules with potential biological activity. Researchers often employ it in the synthesis of heterocyclic compounds that are explored for their therapeutic properties, particularly in areas such as antimicrobial, antiviral, and anticancer drug development. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse chemical libraries for high-throughput screening in drug discovery programs.
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