CAS 1204334-21-3

5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-pyridinediamine

Description:

5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-pyridinediamine is a chemical compound characterized by its unique structure, which includes a pyridine ring and a boron-containing moiety. The presence of the dioxaborolane group contributes to its potential reactivity and utility in various chemical reactions, particularly in organic synthesis and medicinal chemistry. This compound may exhibit properties such as solubility in polar organic solvents, and its boron atom can participate in coordination chemistry, making it useful in the development of boron-based reagents. Additionally, the amine groups in the pyridine ring can engage in hydrogen bonding and may influence the compound's biological activity. The compound's specific applications could range from being a building block in drug development to serving as a ligand in coordination complexes. As with many boron-containing compounds, it may also have implications in materials science and catalysis. Safety and handling precautions should be observed due to the potential reactivity of its functional groups.

Formula: C₁₁H₁₈BN₃O₂

InChI: InChI=1S/C11H18BN3O2/c1-10(2)11(3,4)17-12(16-10)7-5-8(13)9(14)15-6-7/h5-6H,13H2,1-4H3,(H2,14,15)

InChI key: InChIKey=XYAJKHYERTYNDS-UHFFFAOYSA-N

SMILES: CC1(C)OB(OC1(C)C)C=2C=C(N)C(N)=NC2

Synonyms:

• 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-pyridinediamine
• 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-2,3-diamine
• 2,3-Pyridinediamine, 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
• 5,6-DiaMinopyridine-3-boronic acid pinacol ester, 97%
• 5-(4,4,5,5-Tetramethyl-1,3,2dioxaborolan-2-yl)-pyridine-2,3-diamine