5-Bromo-4-chloro-6-iodothieno[2,3-d]pyrimidine
97%
- Product Code: 49005
CAS:
1799610-89-1
| Molecular Weight: | 375.41 g./mol | Molecular Formula: | C₆HBrClIN₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30728471 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, protected from light and stored in an inert gas |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry and drug discovery. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting specific enzymes or receptors. Its unique structure allows for the development of potential therapeutic agents, especially in the treatment of diseases such as cancer, where it can be incorporated into molecules designed to inhibit tumor growth. Additionally, it is used in research to study structure-activity relationships, helping scientists optimize the efficacy and selectivity of new drug candidates. Its halogenated thienopyrimidine core makes it a versatile building block in organic synthesis, enabling the creation of diverse chemical libraries for high-throughput screening.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,026.00 |
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| 0.250 | 10-20 days | ฿1,521.00 |
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| 1.000 | 10-20 days | ฿4,338.00 |
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| 5.000 | 10-20 days | ฿17,037.00 |
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5-Bromo-4-chloro-6-iodothieno[2,3-d]pyrimidine
This chemical is primarily utilized in the field of medicinal chemistry and drug discovery. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting specific enzymes or receptors. Its unique structure allows for the development of potential therapeutic agents, especially in the treatment of diseases such as cancer, where it can be incorporated into molecules designed to inhibit tumor growth. Additionally, it is used in research to study structure-activity relationships, helping scientists optimize the efficacy and selectivity of new drug candidates. Its halogenated thienopyrimidine core makes it a versatile building block in organic synthesis, enabling the creation of diverse chemical libraries for high-throughput screening.
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