(2-(Methoxycarbonyl)-5-(trifluoromethyl)phenyl)boronic acid

97%

  • Product Code: 87043
  CAS:    1217500-62-3
Molecular Weight: 247.96 g./mol Molecular Formula: C₉H₈BF₃O₄
EC Number: MDL Number: MFCD12025964
Melting Point: Boiling Point: 369.0±52.0 °C(Predicted)
Density: 1.41±0.1 g/cm3(Predicted) Storage Condition: 2-8°C, inert gas
Product Description: This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for the introduction of trifluoromethyl-substituted aromatic structures into more complex molecules. The presence of the boronic acid group enables efficient coupling with aryl halides, while the trifluoromethyl group enhances the chemical and metabolic stability of the resulting compounds. Applications include the development of pharmaceuticals, agrochemicals, and advanced materials, where the trifluoromethyl group imparts desirable properties such as increased lipophilicity and resistance to degradation. Additionally, it is used in the synthesis of bioactive molecules and in medicinal chemistry research for drug discovery and optimization.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿1,971.00
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0.250 10-20 days ฿3,339.00
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1.000 10-20 days ฿9,000.00
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(2-(Methoxycarbonyl)-5-(trifluoromethyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for the introduction of trifluoromethyl-substituted aromatic structures into more complex molecules. The presence of the boronic acid group enables efficient coupling with aryl halides, while the trifluoromethyl group enhances the chemical and metabolic stability of the resulting compounds. Applications include the development of pharmaceuticals, agrochemicals, and advanced materials, where the trifluoromethyl group imparts desirable properties such as increased lipophilicity and resistance to degradation. Additionally, it is used in the synthesis of bioactive molecules and in medicinal chemistry research for drug discovery and optimization.
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