17326-31-7

Basic information

• Product Name: 2-(morpholin-4-yl)-4H-pyrido[1,2-a]pyrimidin-4-one
• Synonyms: 4H-pyrido[1,2-a]pyrimidin-4-one, 2-(4-morpholinyl)-
• CAS NO: 17326-31-7
• Molecular Formula: C₁₂H₁₃N₃O₂
• Molecular Weight: 231.2505
• Mol File: 17326-31-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 395.7°C at 760 mmHg
• Flash Point: 193.1°C
• Density: 1.35g/cm³
• Vapor Pressure: 1.81E-06mmHg at 25°C
• Refractive Index: 1.666
• CAS DataBase Reference: 2-(morpholin-4-yl)-4H-pyrido[1,2-a]pyrimidin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(morpholin-4-yl)-4H-pyrido[1,2-a]pyrimidin-4-one(17326-31-7)
• EPA Substance Registry System: 2-(morpholin-4-yl)-4H-pyrido[1,2-a]pyrimidin-4-one(17326-31-7)

Safety Data

• Hazardous Substances Data: 17326-31-7(Hazardous Substances Data)

Usage

Derivative of pyrido[1,2-a]pyrimidin-4-one

Heterocyclic compound with potential biological activity

Contains a morpholine ring

A five-membered ring containing four carbon atoms and one nitrogen atom

Contains a pyrido[1,2-a]pyrimidin-4-one core structure

A central structure that contributes to the compound's potential pharmacological activity

Potential pharmacophore

A compound that can be used as a starting point for drug design due to its potential biological activity

Limited documentation of chemical properties

The specific chemical properties of 2-(morpholin-4-yl)-4H-pyrido[1,2-a]pyrimidin-4-one have not been widely studied

Limited documentation of pharmacological activities

The pharmacological activities of 2-(morpholin-4-yl)-4H-pyrido[1,2-a]pyrimidin-4-one have not been widely studied

Potential for pharmaceutical research and development

Due to its unique structure and potential biological activity, 2-(morpholin-4-yl)-4H-pyrido[1,2-a]pyrimidin-4-one holds promise for further research and development in the field of pharmaceuticals.

Upstream product

• 302326-01-8 2-morpholino-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carbaldehyde 
• 17481-62-8 2-chloro-4-oxo-4H-pyrido<1,2-a>pyrimidine 3-carboxaldehyde 
• 504-29-0 2-aminopyridine 
• 37714-64-0 3-(4-Morpholinyl)-3-oxopropansaeure-ethylester 
• 110-91-8 morpholine 
• 5418-94-0 2-chloro-4H-pyrido[1,2-a]pyrimidin-4-one 

Relevant articles and documents

Generation of functionalized azomethine ylides and their application to stereoselective heterocycle synthesis: an equivalent process of C-unsubstituted nitrile ylide cycloaddition reaction

The synthetic process equivalent to C-unsubstituted (CH) nitrile ylides cycloaddition reaction is achieved via cycloaddition of NH-azomethine ylide and the following fission reaction of the cycloadducts under acidic conditions. Cycloaddition of NH-azometh