3-(4-Bromothiazol-5-yl)phenylboronic acid pinacol ester

95%

  • Product Code: 89982
  CAS:    2223032-07-1
Molecular Weight: 384.09626 g./mol Molecular Formula: C₁₅H₁₉BBrNO₃S
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: -20°C, sealed, dry
Product Description: This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of biaryl structures. This makes it valuable in the development of drugs, functional materials, and advanced chemical compounds. Additionally, its thiazole moiety contributes to its application in designing biologically active molecules, including potential therapeutic agents targeting various diseases.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.005 10-20 days £227.98
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0.025 10-20 days £662.77
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3-(4-Bromothiazol-5-yl)phenylboronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of biaryl structures. This makes it valuable in the development of drugs, functional materials, and advanced chemical compounds. Additionally, its thiazole moiety contributes to its application in designing biologically active molecules, including potential therapeutic agents targeting various diseases.
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