5-Bromoisothiazolo[3,4-b]pyridin-3-amine
97%
- Product Code: 120249
CAS:
1823368-22-4
| Molecular Weight: | 230.09 g./mol | Molecular Formula: | C₆H₄BrN₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26939235 | |
| Melting Point: | Boiling Point: | 368.8°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various heterocyclic compounds, which are often explored for their potential biological activities. Researchers focus on its incorporation into drug discovery projects, particularly in the development of small molecule inhibitors targeting specific enzymes or receptors. Its structural framework is valuable in designing compounds with potential therapeutic applications, such as anti-inflammatory, antimicrobial, or anticancer agents. Additionally, it is studied for its role in modifying the pharmacokinetic properties of drug candidates, enhancing their efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $258.73 |
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| 0.250 | 10-20 days | $452.68 |
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| 1.000 | 10-20 days | $1,133.30 |
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5-Bromoisothiazolo[3,4-b]pyridin-3-amine
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various heterocyclic compounds, which are often explored for their potential biological activities. Researchers focus on its incorporation into drug discovery projects, particularly in the development of small molecule inhibitors targeting specific enzymes or receptors. Its structural framework is valuable in designing compounds with potential therapeutic applications, such as anti-inflammatory, antimicrobial, or anticancer agents. Additionally, it is studied for its role in modifying the pharmacokinetic properties of drug candidates, enhancing their efficacy and selectivity.
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