7-Chloro-6-nitrothieno[3,2-b]pyridine
≥95%
- Product Code: 120846
CAS:
110651-92-8
| Molecular Weight: | 214.63 g./mol | Molecular Formula: | C₇H₃ClN₂O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26383548 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
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 pharmaceuticals and bioactive compounds. Its unique structure allows it to participate in reactions that form complex molecules, particularly those with potential therapeutic properties. Researchers often employ it in the synthesis of heterocyclic compounds, which are crucial in drug discovery for treating diseases such as cancer, infections, and neurological disorders. Additionally, its nitro and chloro functional groups make it a versatile building block for further chemical modifications, enabling the creation of diverse derivatives with tailored biological activities. Its application extends to the study of structure-activity relationships, aiding in the optimization of drug candidates for enhanced efficacy and reduced side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,156.00 |
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| 0.250 | 10-20 days | ฿12,321.00 |
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7-Chloro-6-nitrothieno[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 pharmaceuticals and bioactive compounds. Its unique structure allows it to participate in reactions that form complex molecules, particularly those with potential therapeutic properties. Researchers often employ it in the synthesis of heterocyclic compounds, which are crucial in drug discovery for treating diseases such as cancer, infections, and neurological disorders. Additionally, its nitro and chloro functional groups make it a versatile building block for further chemical modifications, enabling the creation of diverse derivatives with tailored biological activities. Its application extends to the study of structure-activity relationships, aiding in the optimization of drug candidates for enhanced efficacy and reduced side effects.
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