1315351-02-0

Basic information

• Product Name: 6-(piperidin-1-yl)pyridin-2-ylboronic acid
• Synonyms: 6-(piperidin-1-yl)pyridin-2-ylboronic acid
• CAS NO: 1315351-02-0
• Molecular Formula: C10H15BN2O2
• Molecular Weight: 206.0493
• Mol File: 1315351-02-0.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 443.0±55.0 °C(Predicted)
• Appearance: /
• Density: 1.21±0.1 g/cm3(Predicted)
• Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
• PKA: 6.83±0.53(Predicted)
• CAS DataBase Reference: 6-(piperidin-1-yl)pyridin-2-ylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(piperidin-1-yl)pyridin-2-ylboronic acid(1315351-02-0)
• EPA Substance Registry System: 6-(piperidin-1-yl)pyridin-2-ylboronic acid(1315351-02-0)

Safety Data

• Hazardous Substances Data: 1315351-02-0(Hazardous Substances Data)

Usage

Description

(6-(Piperidin-1-yl)pyridin-2-yl)boronic acid is a boronic acid derivative featuring a piperidine ring and a pyridine ring. This chemical compound is widely recognized for its utility in organic synthesis, particularly as a reagent for cross-coupling reactions like the Suzuki-Miyaura coupling. Its unique structure, which includes the boronic acid moiety, enables selective binding to specific biological targets, positioning it as a promising candidate in medicinal chemistry and drug discovery. Furthermore, it has been explored for its potential anti-cancer and anti-inflammatory properties, adding to its significance in the pharmaceutical industry.

Uses

Used in Pharmaceutical Industry:
(6-(Piperidin-1-yl)pyridin-2-yl)boronic acid is used as a reagent for cross-coupling reactions, such as the Suzuki-Miyaura coupling, to modify the structure of organic molecules and create new pharmaceutical compounds. Its ability to selectively bind to certain biological targets makes it a valuable tool in the development of potential drug candidates.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (6-(Piperidin-1-yl)pyridin-2-yl)boronic acid is utilized as a structural modifier to enhance the properties of existing compounds or create novel ones. Its versatility in binding to specific biological targets aids in the advancement of drug discovery and design.
Used in Drug Development:
(6-(Piperidin-1-yl)pyridin-2-yl)boronic acid is employed in the development of potential drug candidates due to its selective binding capabilities. This feature is crucial in identifying and targeting specific biological pathways or receptors, which can lead to the creation of more effective and targeted therapeutics.
Used in Anti-Cancer Research:
This boronic acid derivative is investigated for its potential anti-cancer activities. Its ability to selectively bind to biological targets makes it a promising compound for the development of new cancer treatments, particularly if its interactions can be leveraged to disrupt cancer cell signaling or inhibit tumor growth.
Used in Anti-Inflammatory Applications:
(6-(Piperidin-1-yl)pyridin-2-yl)boronic acid has also been explored for its potential anti-inflammatory properties. If successful, it could be used as a therapeutic agent to alleviate inflammation, which is a common factor in various diseases and conditions.