CAS 269410-03-9
:phenyl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanone
Description:
Phenyl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanone, identified by its CAS number 269410-03-9, is an organic compound characterized by its complex structure that includes a phenyl group and a dioxaborolane moiety. This compound typically exhibits properties associated with both aromatic and boron-containing compounds, which can influence its reactivity and stability. The presence of the dioxaborolane group suggests potential applications in organic synthesis, particularly in cross-coupling reactions, due to the boron atom's ability to participate in various chemical transformations. Additionally, the compound may display unique optical properties owing to its aromatic nature, making it of interest in materials science and photonics. Its solubility and stability in various solvents can vary, depending on the specific conditions and the presence of substituents. Overall, this compound represents a versatile building block in organic chemistry, with potential applications in pharmaceuticals, agrochemicals, and advanced materials.
Formula:C19H21BO3
InChI:InChI=1/C19H21BO3/c1-18(2)19(3,4)23-20(22-18)16-12-10-15(11-13-16)17(21)14-8-6-5-7-9-14/h5-13H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccc(cc2)C(=O)c2ccccc2)O1
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Found 4 products.
4-(Phenylcarbonyl)phenylboronic acid, pinacol ester
CAS:Formula:C19H21BO3Purity:95%Color and Shape:SolidMolecular weight:308.1792Phenyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanone
CAS:<p>Phenyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanone</p>Purity:95%Molecular weight:308.18g/molPhenyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanone
CAS:Purity:95%Molecular weight:308.17999274-(Phenylcarbonyl)phenylboronic acid, pinacol ester
CAS:<p>Versatile small molecule scaffold</p>Formula:C19H21BO3Purity:Min. 95%Molecular weight:308.18 g/mol



