CAS 1251537-33-3

N-CBZ-1,2,3,6-tetrahydropyridin-4-ylboronic acid

Description:

N-CBZ-1,2,3,6-tetrahydropyridin-4-ylboronic acid is a boronic acid derivative characterized by the presence of a tetrahydropyridine ring, which contributes to its unique chemical properties. The "N-CBZ" designation indicates that the nitrogen atom in the tetrahydropyridine is protected by a carbobenzyloxy (CBZ) group, enhancing its stability and solubility in organic solvents. This compound typically exhibits a polar nature due to the boronic acid functional group, which can participate in reversible covalent bonding with diols, making it useful in various applications, including medicinal chemistry and organic synthesis. The boronic acid moiety also allows for potential interactions with biological targets, making it a candidate for drug development. Additionally, the compound's structure suggests it may have specific reactivity patterns, such as undergoing Suzuki coupling reactions, which are valuable in forming carbon-carbon bonds. Overall, N-CBZ-1,2,3,6-tetrahydropyridin-4-ylboronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.

Formula: C₁₃H₁₆BNO₄

Synonyms:

• N-CBZ-1,2,3,6-tetrahydropyridin-4-ylboronic acid
• N-CBZ-1,2,3,6-tetrahydropyridin-4-ylboronic acid ISO 9001：2015 REACH
• 1-(benzyloxycarbonyl)-1,2,3,6-tetrahydropyridin-4-ylboronic acid
• (1-phenylmethoxycarbonyl-3,6-dihydro-2H-pyridin-4-yl)boronicaci
• 1(2H)-Pyridinecarboxylic acid, 4-borono-3,6-dihydro-, 1-(phenylmethyl) ester
• [1-Cbz-1,2,3,6-tetrahydropyridine-4-yl]boronic acid

{1-[(benzyloxy)carbonyl]-1,2,3,6-tetrahydropyridin-4-yl}boronic acid

CAS: 1251537-33-3

Formula: C₁₃H₁₆BNO₄

Molecular weight: 261.0814

Ref: IN-DA000N93