CAS 1073354-65-0: 2-(5-Chloro-2,4-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description: 2-(5-Chloro-2,4-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique dioxaborolane structure, which features a five-membered ring containing boron and oxygen atoms. This compound exhibits a high degree of steric hindrance due to the presence of four methyl groups, which can influence its reactivity and solubility. The chlorinated and difluorinated phenyl group contributes to its electronic properties, potentially enhancing its reactivity in various chemical reactions, such as Suzuki coupling, which is commonly used in organic synthesis. The presence of halogen substituents can also affect the compound's lipophilicity and biological activity. Additionally, the compound's stability and reactivity can be influenced by environmental factors such as temperature and solvent polarity. Overall, this compound is of interest in the field of medicinal chemistry and materials science, particularly for applications involving boron chemistry and the development of new synthetic methodologies.

Formula: C₁₂H₁₄BClF₂O₂

InChI: InChI=1S/C12H14BClF2O2/c1-11(2)12(3,4)18-13(17-11)7-5-8(14)10(16)6-9(7)15/h5-6H,1-4H3

InChI key: InChIKey=BSMXVFVYXLZVKL-UHFFFAOYSA-N

SMILES: FC=1C=C(F)C(=CC1Cl)B2OC(C)(C)C(O2)(C)C

5-Chloro-2,4-difluorophenylboronic acid pinacol ester

CAS: 1073354-65-0

• Formula: C₁₂H₁₄BClF₂O₂
• Purity: 97%
• Color and Shape: Solid
• Molecular weight: 274.4992

5-Chloro-2,4-difluorobenzeneboronic acid pinacol ester

CAS: 1073354-65-0

• Molecular weight: 274.50g/mol

2-(5-Chloro-2,4-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 1073354-65-0

• Purity: 97%
• Molecular weight: 274.5