CAS 736989-88-1

1,1-Dimethylethyl N-[2-oxo-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethyl]carbamate

Description:

1,1-Dimethylethyl N-[2-oxo-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethyl]carbamate, with CAS number 736989-88-1, is a chemical compound characterized by its complex structure, which includes a carbamate functional group and a boron-containing moiety. This compound features a dimethyl group that enhances its steric properties, making it potentially useful in various chemical applications, including as a reagent or intermediate in organic synthesis. The presence of the dioxaborolane ring suggests that it may exhibit unique reactivity patterns, particularly in cross-coupling reactions or as a boron source in organic transformations. Additionally, the phenyl group attached to the dioxaborolane may contribute to its electronic properties, influencing its behavior in chemical reactions. Overall, this compound's unique structural features may provide opportunities for applications in medicinal chemistry, materials science, or as a catalyst in organic reactions, although specific applications would depend on further research and characterization.

Formula: C₁₉H₂₈BNO₅

InChI: InChI=1S/C19H28BNO5/c1-17(2,3)24-16(23)21-12-15(22)13-8-10-14(11-9-13)20-25-18(4,5)19(6,7)26-20/h8-11H,12H2,1-7H3,(H,21,23)

InChI key: InChIKey=ATQJBOSFTLBQHM-UHFFFAOYSA-N

SMILES: CC1(C)OB(OC1(C)C)C2=CC=C(C(CNC(OC(C)(C)C)=O)=O)C=C2

Synonyms:

• 2-(N-tert-Butoxycarbonylamino)-1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethanone
• Carbamic acid, [2-oxo-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethyl]-, 1,1-dimethylethyl ester
• 1,1-Dimethylethyl N-[2-oxo-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethyl]carbamate
• [2-Oxo-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethyl]Carbamic acid 1,1-dimethylethyl ester
• Carbamic acid, N-[2-oxo-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethyl]-, 1,1-dimethylethyl ester