(2-((tert-Butoxycarbonyl)amino)-7-fluorobenzo[d]thiazol-4-yl)boronic acid
97%
- Product Code: 88996
CAS:
2415163-55-0
Molecular Weight: | 312.12 g./mol | Molecular Formula: | C₁₂H₁₄BFN₂O₄S |
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EC Number: | MDL Number: | MFCD32689945 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the preparation of complex molecules, especially in the pharmaceutical industry. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing biologically active compounds. The fluorobenzo[d]thiazole moiety is often incorporated into drug candidates targeting various diseases, including cancer and neurological disorders. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective modifications during multi-step synthetic processes, enhancing its versatility in medicinal chemistry research.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿7,065.00 |
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0.250 | 10-20 days | ฿10,620.00 |
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1.000 | 10-20 days | ฿26,640.00 |
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(2-((tert-Butoxycarbonyl)amino)-7-fluorobenzo[d]thiazol-4-yl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the preparation of complex molecules, especially in the pharmaceutical industry. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing biologically active compounds. The fluorobenzo[d]thiazole moiety is often incorporated into drug candidates targeting various diseases, including cancer and neurological disorders. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective modifications during multi-step synthetic processes, enhancing its versatility in medicinal chemistry research.
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