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CAS 262433-02-3

:

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

Description:
1,1-Dimethylethyl N-[2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate, with CAS number 262433-02-3, 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 reactions and applications. The presence of the methoxy and phenyl groups contributes to its solubility and reactivity, while the dioxaborolane ring is known for its role in facilitating boron-mediated reactions, such as cross-coupling processes in organic synthesis. The compound's unique structure may impart specific biological or chemical activities, making it of interest in fields such as medicinal chemistry or materials science. As with many synthetic organic compounds, its stability, reactivity, and potential applications would depend on the specific conditions under which it is used, including solvent choice, temperature, and the presence of other reagents.
Formula:C18H28BNO5
InChI:InChI=1S/C18H28BNO5/c1-16(2,3)23-15(21)20-13-10-9-12(11-14(13)22-8)19-24-17(4,5)18(6,7)25-19/h9-11H,1-8H3,(H,20,21)
InChI key:InChIKey=HTNAUNFQAMHASO-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(OC)=C(NC(OC(C)(C)C)=O)C=C2
Synonyms:
  • 1,1-Dimethylethyl N-[2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate
  • 4-(tert-Butoxycarbonylamino)-3-methoxyphenylboronic acid, pinacol ester
  • Carbamic acid, N-[2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-, 1,1-dimethylethyl ester
  • Carbamic acid, [2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-, 1,1-dimethylethyl ester
  • tert-Butyl N-[2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate
  • tert-Butyl (2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
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