2-Quinolin-3-ylethanamine, identified by its CAS number 776333-52-9, is an organic compound that features a quinoline moiety, which is a bicyclic structure composed of a benzene ring fused to a pyridine ring. This compound typically exhibits characteristics common to amines, such as basicity and the ability to form hydrogen bonds due to the presence of the amino group (-NH2). The quinoline structure contributes to its potential biological activity, making it of interest in medicinal chemistry. It may exhibit various pharmacological properties, including antimicrobial or antitumor activities, depending on its specific substituents and structural context. The compound is likely to be soluble in polar solvents, and its reactivity can be influenced by the electron-donating or withdrawing nature of substituents on the quinoline ring. Additionally, it may participate in various chemical reactions typical of amines, such as alkylation or acylation. Overall, 2-quinolin-3-ylethanamine represents a versatile scaffold for further chemical modifications and potential applications in drug development.

2-quinolin-3-ylethanamine

776333-52-9: 2-Quinolin-3-ylethanamine, identified by its CAS number 776333-52-9, is an organic compound that features a quinoline moiety, which is a bicyclic structure composed of a benzene ring fused to a pyridine ring. This compound typically exhibits characteristics common to amines, such as basicity and the ability to form hydrogen bonds due to the presence of the amino group (-NH2). The quinoline structure contributes to its potential biological activity, making it of interest in medicinal chemistry. It may exhibit various pharmacological properties, including antimicrobial or antitumor activities, depending on its specific substituents and structural context. The compound is likely to be soluble in polar solvents, and its reactivity can be influenced by the electron-donating or withdrawing nature of substituents on the quinoline ring. Additionally, it may participate in various chemical reactions typical of amines, such as alkylation or acylation. Overall, 2-quinolin-3-ylethanamine represents a versatile scaffold for further chemical modifications and potential applications in drug development.

CAS 776333-52-9

2-quinolin-3-ylethanamine

2-(Quinolin-3-yl)ethanamine

Ref: IN-DA005SLR

2-(Quinolin-3-yl)ethan-1-amine

Ref: 3D-BGB33352