CAS 135323-95-4: 2-CHLORO-4-(MORPHOLIN-4-YLCARBONYL)QUINOLINE

Description: 2-Chloro-4-(morpholin-4-ylcarbonyl)quinoline is a chemical compound characterized by its quinoline backbone, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. The presence of a chloro substituent at the 2-position and a morpholin-4-ylcarbonyl group at the 4-position contributes to its unique chemical properties. This compound is typically classified as an aromatic heterocycle due to the nitrogen atom in the quinoline structure. It may exhibit biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The morpholine moiety can enhance solubility and bioavailability, while the chloro group may influence reactivity and interaction with biological targets. Its molecular structure suggests potential applications in drug design, particularly in targeting specific enzymes or receptors. As with many organic compounds, its stability, solubility, and reactivity can be influenced by environmental conditions such as pH and temperature. Safety and handling precautions are essential when working with this compound, as with any chemical substance.

Formula: C₁₄H₁₃ClN₂O₂

InChI: InChI=1/C14H13ClN2O2/c15-13-9-11(10-3-1-2-4-12(10)16-13)14(18)17-5-7-19-8-6-17/h1-4,9H,5-8H2

Synonyms:

• (2-Chloro-quinolin-4-yl)-morpholin-4-yl-methanone
• Methanone, (2-chloro-4-quinolinyl)-4-morpholinyl-

2-Chloro-4-(morpholine-4-carbonyl)quinoline

CAS: 135323-95-4

Versatile small molecule scaffold

• Formula: C₁₄H₁₃ClN₂O₂
• Purity: Min. 95%
• Molecular weight: 276.72 g/mol

2-Chloro-4-(morpholine-4-carbonyl)quinoline

CAS: 135323-95-4

• Purity: 98+%
• Molecular weight: 276.7200012207031