CAS 874291-03-9
:1-isobutyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea
Description:
1-Isobutyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea, with the CAS number 874291-03-9, is a chemical compound characterized by its unique structure that includes a urea functional group and a boron-containing moiety. This compound features an isobutyl group, which contributes to its hydrophobic characteristics, and a phenyl ring that is substituted with a boron-containing dioxaborolane, enhancing its potential for applications in organic synthesis and materials science. The presence of the dioxaborolane unit suggests potential reactivity in cross-coupling reactions, making it valuable in the development of pharmaceuticals and agrochemicals. Additionally, the compound's structural features may influence its solubility, stability, and interaction with biological systems. Overall, this compound exemplifies the integration of boron chemistry into organic molecules, which can lead to innovative applications in various fields, including medicinal chemistry and polymer science.
Formula:C17H27BN2O3
InChI:InChI=1/C17H27BN2O3/c1-12(2)11-19-15(21)20-14-9-7-13(8-10-14)18-22-16(3,4)17(5,6)23-18/h7-10,12H,11H2,1-6H3,(H2,19,20,21)
SMILES:CC(C)CN=C(Nc1ccc(cc1)B1OC(C)(C)C(C)(C)O1)O
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Found 3 products.
4-(3-Isobutylureido)phenylboronic acid, pinacol ester
CAS:Formula:C17H27BN2O3Purity:95%Color and Shape:SolidMolecular weight:318.21894-[(Isobutylcarbamoyl)amino]benzeneboronic acid, pinacol ester
CAS:<p>4-[(Isobutylcarbamoyl)amino]benzeneboronic acid, pinacol ester</p>Purity:98%Molecular weight:318.22g/mol1-Isobutyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
CAS:Purity:98%Molecular weight:318.2200012


