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CAS 1565857-69-3

:

4,4,5,5-Tetramethyl-2-(4-nitro-1-naphthalenyl)-1,3,2-dioxaborolane

Description:
4,4,5,5-Tetramethyl-2-(4-nitro-1-naphthalenyl)-1,3,2-dioxaborolane is an organoboron compound characterized by its unique boron-containing dioxaborolane ring structure, which contributes to its reactivity and stability. The presence of the nitro group on the naphthalene moiety enhances its electron-withdrawing properties, making it useful in various chemical applications, including organic synthesis and materials science. The tetramethyl substituents provide steric hindrance, which can influence the compound's reactivity and solubility in organic solvents. This compound is typically used in cross-coupling reactions, particularly in the formation of carbon-carbon bonds, and may serve as a precursor for the synthesis of more complex organic molecules. Its specific properties, such as melting point, boiling point, and solubility, can vary based on the solvent and conditions used. Overall, 4,4,5,5-Tetramethyl-2-(4-nitro-1-naphthalenyl)-1,3,2-dioxaborolane is a valuable compound in synthetic organic chemistry, particularly in the development of functionalized materials and pharmaceuticals.
Formula:C16H18BNO4
InChI:InChI=1S/C16H18BNO4/c1-15(2)16(3,4)22-17(21-15)13-9-10-14(18(19)20)12-8-6-5-7-11(12)13/h5-10H,1-4H3
InChI key:InChIKey=CPUXTQDJTZGHRK-UHFFFAOYSA-N
SMILES:N(=O)(=O)C=1C2=C(C(=CC1)B3OC(C)(C)C(C)(C)O3)C=CC=C2
Synonyms:
  • 4,4,5,5-Tetramethyl-2-(4-nitro-1-naphthalenyl)-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(4-nitro-1-naphthalenyl)-
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