1241253-40-6

Basic information

• Product Name: [1-(2-Fluoro-benzyl)-piperidin-4-yl]-methanol
• Synonyms: [1-(2-Fluoro-benzyl)-piperidin-4-yl]-methanol
• CAS NO: 1241253-40-6
• Molecular Formula: C13H18FNO
• Molecular Weight: 223.2865232
• Mol File: 1241253-40-6.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: [1-(2-Fluoro-benzyl)-piperidin-4-yl]-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: [1-(2-Fluoro-benzyl)-piperidin-4-yl]-methanol(1241253-40-6)
• EPA Substance Registry System: [1-(2-Fluoro-benzyl)-piperidin-4-yl]-methanol(1241253-40-6)

Safety Data

• Hazardous Substances Data: 1241253-40-6(Hazardous Substances Data)

Usage

Description

[1-(2-Fluoro-benzyl)-piperidin-4-yl]-methanol is a chemical compound belonging to the piperidine family, characterized by a piperidine ring with a fluoro-benzyl substituent at the 1-position and a methanol group at the 4-position. [1-(2-Fluoro-benzyl)-piperidin-4-yl]-methanol holds promise in medicinal chemistry for its potential role in the development of pharmaceutical drugs, with the fluoro-benzyl group possibly imparting unique biological activities and the methanol group offering opportunities for chemical modifications or conjugations.

Uses

Used in Pharmaceutical Development:
[1-(2-Fluoro-benzyl)-piperidin-4-yl]-methanol is used as a key intermediate in the synthesis of pharmaceutical drugs due to its unique structural features. The presence of the fluoro-benzyl group may enhance the compound's biological activity, while the methanol group allows for further chemical modifications to optimize drug properties such as solubility, stability, and bioavailability.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, [1-(2-Fluoro-benzyl)-piperidin-4-yl]-methanol serves as a valuable compound for research and investigation. Its structural attributes make it a candidate for exploring new drug mechanisms, targeting specific biological pathways, and potentially leading to the creation of novel therapeutic agents.
Used in Drug Conjugation and Modification:
The methanol group in [1-(2-Fluoro-benzyl)-piperidin-4-yl]-methanol can be utilized for drug conjugation and modification, allowing for the attachment of various functional groups or other molecules. This can result in the development of prodrugs or drug delivery systems with improved pharmacokinetic and pharmacodynamic profiles.
Note: Since the provided materials do not specify particular applications or industries for [1-(2-Fluoro-benzyl)-piperidin-4-yl]-methanol, the uses listed are general and based on the potential of the compound's structure and properties in medicinal chemistry and pharmaceutical development. Further research would be necessary to identify specific applications and industries.