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 |
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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 (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿540.00 |
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1.000 | 10-20 days | ฿1,755.00 |
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5.000 | 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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