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CAS 562098-08-2

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4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl acetate

Description:
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl acetate, with the CAS number 562098-08-2, is a chemical compound that features a benzyl acetate moiety linked to a dioxaborolane group. This compound is characterized by its boron-containing structure, which is significant in various chemical reactions, particularly in organic synthesis and catalysis. The presence of the dioxaborolane ring contributes to its stability and reactivity, making it useful in cross-coupling reactions, such as Suzuki reactions, where it can serve as a boron source. The tetramethyl substituents enhance its solubility and steric properties, which can influence its reactivity and interaction with other molecules. Additionally, the acetate group provides a functional handle for further chemical modifications. Overall, this compound exemplifies the integration of boron chemistry with organic functional groups, making it a valuable intermediate in the synthesis of more complex organic molecules.
Formula:C15H21BO4
InChI:InChI=1/C15H21BO4/c1-11(17)18-10-12-6-8-13(9-7-12)16-19-14(2,3)15(4,5)20-16/h6-9H,10H2,1-5H3
SMILES:CC(=O)OCc1ccc(cc1)B1OC(C)(C)C(C)(C)O1
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