(2-(methoxycarbonyl)thiazol-5-yl)boronic acid

95%

  • Product Code: 89011
  CAS:    2256708-88-8
Molecular Weight: 186.98144 g./mol Molecular Formula: C₅H₆BNO₄S
EC Number: MDL Number:
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Density: Storage Condition: -20°C, sealed, dry
Product Description: (2-(Methoxycarbonyl)thiazol-5-yl)boronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules, including drug candidates. The compound acts as a boronic acid reagent, facilitating the introduction of the thiazole moiety into target molecules. Thiazole derivatives are known for their biological activity, making this chemical valuable in the development of potential therapeutic agents. Additionally, it may be used in material science for the preparation of functionalized organic materials, where the thiazole ring can impart specific electronic or structural properties. Its application in these fields highlights its role as a versatile building block in both medicinal chemistry and advanced materials research.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.025 10-20 days ฿86,000.00
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0.100 10-20 days ฿258,000.00
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(2-(methoxycarbonyl)thiazol-5-yl)boronic acid
(2-(Methoxycarbonyl)thiazol-5-yl)boronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules, including drug candidates. The compound acts as a boronic acid reagent, facilitating the introduction of the thiazole moiety into target molecules. Thiazole derivatives are known for their biological activity, making this chemical valuable in the development of potential therapeutic agents. Additionally, it may be used in material science for the preparation of functionalized organic materials, where the thiazole ring can impart specific electronic or structural properties. Its application in these fields highlights its role as a versatile building block in both medicinal chemistry and advanced materials research.
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