353257-77-9

Basic information

• Product Name: 1-(3-Chloro-quinoxalin-2-yl)-piperidin-4-ol, 98+% C13H14ClN3O, MW: 263.72
• Synonyms: 1-(3-Chloro-quinoxalin-2-yl)-piperidin-4-ol, 98+% C13H14ClN3O, MW: 263.72
• CAS NO: 353257-77-9
• Molecular Formula: C13H14ClN3O
• Molecular Weight: 263.72276
• Mol File: 353257-77-9.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Density: 1.379
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-(3-Chloro-quinoxalin-2-yl)-piperidin-4-ol, 98+% C13H14ClN3O, MW: 263.72(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-Chloro-quinoxalin-2-yl)-piperidin-4-ol, 98+% C13H14ClN3O, MW: 263.72(353257-77-9)
• EPA Substance Registry System: 1-(3-Chloro-quinoxalin-2-yl)-piperidin-4-ol, 98+% C13H14ClN3O, MW: 263.72(353257-77-9)

Safety Data

• Hazardous Substances Data: 353257-77-9(Hazardous Substances Data)

Usage

Description

1-(3-Chloro-quinoxalin-2-yl)-piperidin-4-ol, 98+% C13H14ClN3O, MW: 263.72 is a piperidine derivative featuring a chloro-substituted quinoxaline ring. This chemical compound, with a molecular formula of C13H14ClN3O and a molecular weight of 263.72, is known for its purity of 98% or higher. Its unique structure and properties render it a promising candidate for pharmaceutical research and development, as well as a valuable building block for the synthesis of novel pharmaceutical compounds.

Uses

Used in Pharmaceutical Research and Development:
1-(3-Chloro-quinoxalin-2-yl)-piperidin-4-ol, 98+% C13H14ClN3O, MW: 263.72 is used as a research compound for exploring its potential in drug discovery and medicinal chemistry applications. Its unique structure and functional groups provide opportunities for various chemical transformations, making it a valuable asset in the development of new pharmaceutical agents.
Used in Drug Synthesis:
In the pharmaceutical industry, 1-(3-Chloro-quinoxalin-2-yl)-piperidin-4-ol, 98+% C13H14ClN3O, MW: 263.72 is utilized as a key intermediate in the synthesis of novel pharmaceutical compounds. Its functional groups allow for further chemical modifications, enabling the creation of new drug candidates with potential therapeutic benefits.
Used in Chemical Transformations:
1-(3-Chloro-quinoxalin-2-yl)-piperidin-4-ol, 98+% C13H14ClN3O, MW: 263.72 is employed as a versatile building block in chemical transformations. Its chloro-substituted quinoxaline ring and piperidine moiety offer opportunities for the development of new chemical entities with diverse applications in various fields, including but not limited to pharmaceuticals, agrochemicals, and materials science.