CAS 23443-10-9

4H-Pyrido[1,2-a]pyrimidin-4-one

Description:

4H-Pyrido[1,2-a]pyrimidin-4-one, identified by its CAS number 23443-10-9, is a heterocyclic organic compound featuring a fused pyridine and pyrimidine ring system. This compound typically exhibits a planar structure due to the aromatic nature of its rings, which contributes to its stability and potential reactivity. It is characterized by the presence of a carbonyl group at the 4-position of the pyrimidine ring, which can participate in various chemical reactions, such as nucleophilic attacks. The compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its solubility and reactivity can vary depending on the substituents attached to the ring system. Additionally, 4H-Pyrido[1,2-a]pyrimidin-4-one may serve as a scaffold for the synthesis of more complex molecules, potentially leading to the discovery of new therapeutic agents. Overall, its unique structural features and potential applications make it a subject of interest in both academic and industrial research.

Formula: C₈H₆N₂O

Synonyms:

• Pyrido[1,2-a]pyriMidin-4-one
• pyrido<1,2-a>pyriMidin-4(4H)-one
• CAS:23443-10-9

4H-Pyrido[1,2-a]pyrimidin-4-one

CAS: 23443-10-9

Formula: C₈H₆N₂O

Purity: 98%

Color and Shape: Solid

Molecular weight: 146.1460

Ref: IN-DA002N9I

4H-Pyrido[1,2-a]pyrimidin-4-one

CAS: 23443-10-9

4H-Pyrido[1,2-a]pyrimidin-4-one

Purity: ≥95%

Molecular weight: 146.15g/mol

Ref: 54-OR310030

4H-Pyrido[1,2-a]pyrimidin-4-one

CAS: 23443-10-9

Purity: 98%

Molecular weight: 146.1490021

Ref: 10-F637155

4H-Pyrido[1,2-a]pyrimidin-4-one

CAS: 23443-10-9

4H-Pyrido[1,2-a]pyrimidin-4-one is a sulfonated compound that has various applications. It is commonly used as a preservative in cosmetic and personal care products. Additionally, it has been found to have potential therapeutic effects on iron homeostasis and collagen synthesis. Research suggests that 4H-Pyrido[1,2-a]pyrimidin-4-one can enhance the production of siderophores, which are molecules involved in iron uptake and storage. This compound also exhibits antiplatelet activity, making it a promising candidate for the development of cardiovascular drugs. Furthermore, it has been studied for its role in activating collagen hydrolysate and promoting wound healing. With its versatile properties, 4H-Pyrido[1,2-a]pyrimidin-4-one holds great potential for various scientific and industrial applications.

Formula: C₈H₆N₂O

Purity: Min. 95%

Molecular weight: 146.15 g/mol

Ref: 3D-YAA44310