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Atomfair 2-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride) C7H6BF3O3
Description 2-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride) is a high-purity boronic acid derivative with the molecular formula C7H6BF3O3and CAS number 175676-65-0 . This compound is a valuable building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its reactive boronic acid functional group. The trifluoromethoxy (-OCF3) substituent enhances its utility in pharmaceutical and agrochemical research by imparting unique electronic and steric properties. Our product is rigorously tested for quality, ensuring optimal performance in demanding applications. Available in varying purities, it may contain trace amounts of anhydride, as noted in the product specifications.
Description
Description
2-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride) is a high-purity boronic acid derivative with the molecular formula C7H6BF3O3 and CAS number 175676-65-0. This compound is a valuable building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its reactive boronic acid functional group. The trifluoromethoxy (-OCF3) substituent enhances its utility in pharmaceutical and agrochemical research by imparting unique electronic and steric properties. Our product is rigorously tested for quality, ensuring optimal performance in demanding applications. Available in varying purities, it may contain trace amounts of anhydride, as noted in the product specifications.
- CAS No: 175676-65-0
- Molecular Formula: C7H6BF3O3
- Molecular Weight: 205.93
- Exact Mass: 206.0362087
- Monoisotopic Mass: 206.0362087
- IUPAC Name: [2-(trifluoromethoxy)phenyl]boronic acid
- SMILES: B(C1=CC=CC=C1OC(F)(F)F)(O)O
- Synonyms: 2-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride), 642-456-9, 175676-65-0, 2-(Trifluoromethoxy)phenylboronic acid, 2-Trifluoromethoxyphenylboronic acid
Application
2-(Trifluoromethoxy)phenylboronic Acid is widely used in palladium-catalyzed cross-coupling reactions, such as Suzuki-Miyaura couplings, to synthesize biaryl compounds for pharmaceuticals and materials science. Its trifluoromethoxy group makes it a key intermediate in the development of CF3-containing bioactive molecules, including potential drug candidates. Researchers also employ it in the synthesis of advanced ligands and catalysts for asymmetric transformations.
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