CAS 627525-96-6
:1,3,2-Dioxaborolane, 2-(4-chloro-3-methoxyphenyl)-4,4,5,5-tetramethyl-
Description:
1,3,2-Dioxaborolane, 2-(4-chloro-3-methoxyphenyl)-4,4,5,5-tetramethyl- is an organoboron compound characterized by its dioxaborolane ring structure, which features a five-membered cyclic arrangement containing boron and oxygen atoms. This compound typically exhibits a high degree of stability due to the presence of the boron atom, which can participate in various chemical reactions, including cross-coupling reactions that are valuable in organic synthesis. The presence of the 4-chloro-3-methoxyphenyl substituent contributes to its unique reactivity and potential applications in medicinal chemistry and materials science. The tetramethyl groups enhance the steric bulk around the boron center, influencing its reactivity and solubility properties. Additionally, this compound may exhibit interesting electronic properties due to the electron-withdrawing nature of the chloro group and the electron-donating characteristics of the methoxy group, which can affect its behavior in chemical reactions and interactions with other molecules. Overall, this compound represents a versatile building block in synthetic organic chemistry.
Formula:C13H18BClO3
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Found 3 products.
4-Chloro-3-methoxyphenylboronic acid pinacolester
CAS:Formula:C13H18BClO3Purity:98%Color and Shape:SolidMolecular weight:268.54424-Chloro-3-methoxyphenylboronic acid, pinacol ester
CAS:4-Chloro-3-methoxyphenylboronic acid, pinacol esterPurity:98%Molecular weight:268.54g/mol4-Chloro-3-methoxyphenylboronic acid pinacol ester
CAS:Formula:C13H18BClO3Purity:98%Color and Shape:SolidMolecular weight:268.54


