
CAS 1219931-41-5
:1-(2,2,2-Trifluoroethyl)-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester
Description:
1-(2,2,2-Trifluoroethyl)-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester is a boronic acid derivative characterized by its unique structural features, including a tetrahydropyridine ring and a trifluoroethyl substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the trifluoroethyl group enhances its lipophilicity and may influence its reactivity and solubility in organic solvents. Additionally, the pinacol ester moiety contributes to its stability and can facilitate its use in cross-coupling reactions, a common method in the formation of carbon-carbon bonds. Overall, this compound is of interest in the development of pharmaceuticals and agrochemicals, where its unique functional groups can be leveraged for specific chemical transformations. Its CAS number, 1219931-41-5, allows for easy identification and reference in chemical databases and literature.
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Found 4 products.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(2,2,2-trifluoroethyl)-1,2,3,6-tetrahydropyridine
CAS:Formula:C13H21BF3NO2Purity:95%Color and Shape:SolidMolecular weight:291.11751-(2,2,2-Trifluoroethyl)-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester
CAS:Purity:>95%Molecular weight:291.1181-(2,2,2-Trifluoroethyl)-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester
CAS:1-(2,2,2-Trifluoroethyl)-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol esterPurity:95%Color and Shape:SolidMolecular weight:291.12g/mol1,2,3,6-Tetrahydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(2,2,2-trifluoroethyl)-pyridine
CAS:Purity:95%Molecular weight:291.1199951



