4-Methoxy-3-(trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride)

≥98%

  • Product Code: 77292
  CAS:    149507-36-8
Molecular Weight: 219.95 g./mol Molecular Formula: C₈H₈BF₃O₃
EC Number: MDL Number: MFCD07363790
Melting Point: 202°C Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the coupling of aryl halides with aryl boronic acids to create complex organic compounds. Additionally, it is utilized in the development of bioactive molecules and polymers, contributing to innovations in drug discovery and material science. The presence of the trifluoromethyl group enhances its reactivity and stability, making it suitable for applications requiring precise chemical transformations.
Sizes / Availability / Pricing:
Size Availability Price Quantity
0.250 G 10-20 days ฿540.00
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1.000 G 10-20 days ฿1,755.00
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-
5.000 G 10-20 days ฿6,561.00
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-
4-Methoxy-3-(trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride)
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the coupling of aryl halides with aryl boronic acids to create complex organic compounds. Additionally, it is utilized in the development of bioactive molecules and polymers, contributing to innovations in drug discovery and material science. The presence of the trifluoromethyl group enhances its reactivity and stability, making it suitable for applications requiring precise chemical transformations.
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