6-Bromo-N-methylbenzo[d]thiazol-2-amine
98%
- Product Code: 72603
CAS:
75104-92-6
| Molecular Weight: | 243.12 g./mol | Molecular Formula: | C₈H₇BrN₂S |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various heterocyclic compounds. Its structure, featuring a benzothiazole core, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of molecules with potential therapeutic properties. Researchers often employ it in the creation of compounds that exhibit biological activity, such as antimicrobial, anti-inflammatory, or anticancer agents. Additionally, it is used in the design of fluorescent dyes and imaging agents due to its ability to interact with light, making it useful in biochemical and diagnostic applications. Its versatility in chemical reactions also allows for modifications that can lead to the discovery of new materials with specific electronic or optical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿477.00 |
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| 0.250 | 10-20 days | ฿738.00 |
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| 1.000 | 10-20 days | ฿2,151.00 |
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| 5.000 | 10-20 days | ฿6,507.00 |
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| 10.000 | 10-20 days | ฿11,628.00 |
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6-Bromo-N-methylbenzo[d]thiazol-2-amine
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various heterocyclic compounds. Its structure, featuring a benzothiazole core, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of molecules with potential therapeutic properties. Researchers often employ it in the creation of compounds that exhibit biological activity, such as antimicrobial, anti-inflammatory, or anticancer agents. Additionally, it is used in the design of fluorescent dyes and imaging agents due to its ability to interact with light, making it useful in biochemical and diagnostic applications. Its versatility in chemical reactions also allows for modifications that can lead to the discovery of new materials with specific electronic or optical properties.
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