CAS 1075719-87-7
:2-(4-Ethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Description:
2-(4-Ethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane structure, which features a five-membered ring 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, particularly in organic synthesis and catalysis. The ethylphenyl group contributes to its hydrophobic characteristics, making it less soluble in polar solvents. Additionally, the tetramethyl substituents enhance steric hindrance, which can influence its reactivity and interactions with other molecules. This compound is often utilized in the field of organic chemistry, particularly in Suzuki coupling reactions, where it serves as a boron-containing reagent. Its unique structure and properties make it a valuable intermediate in the synthesis of more complex organic compounds. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C14H21BO2
Synonyms:- 4-Ethylphenylboronic acid pinacol ester
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Found 3 products.
4-Ethylphenylboronic acid pinacol ester
CAS:Formula:C14H21BO2Purity:97%Color and Shape:SolidMolecular weight:232.12634-Ethylphenylboronic acid pinacol ester
CAS:<p>4-Ethylphenylboronic acid pinacol ester</p>Purity:98%Molecular weight:232.13g/mol2-(4-Ethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS:Formula:C14H21BO2Purity:97%Molecular weight:232.13


