(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
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
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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