CAS 132973-43-4

4-(Aminomethyl)-2(1H)-quinolinone

Description:

4-(Aminomethyl)-2(1H)-quinolinone, with the CAS number 132973-43-4, is an organic compound characterized by its quinoline structure, which features a fused bicyclic system containing a nitrogen atom. This compound typically exhibits properties such as being a solid at room temperature and may have moderate solubility in polar solvents due to the presence of the amino group. The amino group (-NH2) contributes to its potential as a building block in medicinal chemistry, particularly in the development of pharmaceuticals, as it can participate in various chemical reactions, including nucleophilic substitutions and hydrogen bonding. Additionally, the quinolinone moiety is known for its biological activity, making this compound of interest in research related to antimicrobial and anticancer agents. Its molecular structure allows for potential interactions with biological targets, which can be explored in drug design and development. Overall, 4-(Aminomethyl)-2(1H)-quinolinone is a compound of significant interest in both synthetic and medicinal chemistry.

Formula: C₁₀H₁₀N₂O

InChI: InChI=1S/C10H10N2O/c11-6-7-5-10(13)12-9-4-2-1-3-8(7)9/h1-5H,6,11H2,(H,12,13)

InChI key: InChIKey=RDXKAGOGKMCTBH-UHFFFAOYSA-N

SMILES: C(N)C=1C=2C(NC(=O)C1)=CC=CC2

Synonyms:

• 2(1H)-Quinolinone, 4-(aminomethyl)-
• 4-(Aminomethyl)-2(1H)-quinolinone
• [(2-Oxo-1,2-dihydroquinolin-4-yl)methyl]amine
• 4-(Aminomethyl)quinolin-2-ol
• 4-(AMINOMETHYL)QUINOLIN-2(1H)-ONE
• 4-(aminomethyl)-1,2-dihydroquinolin-2-one
• 4-(aminomethyl)-1H-quinolin-2-one

4-Aminomethyl-2(1H)-quinolinone

CAS: 132973-43-4

Formula: C₁₀H₁₀N₂O

Purity: 97.0%

Color and Shape: Solid

Molecular weight: 174.203

Ref: 10-F048208

4-Aminomethyl-2(1H)-quinolinone

CAS: 132973-43-4

4-Aminomethyl-2(1H)-quinolinone is an anti-cancer agent that inhibits viral replication. It has been shown to be a potent inhibitor of HIV replication, and has been used in the treatment of AIDS patients. 4-Aminomethyl-2(1H)-quinolinone also inhibits the growth of tumor cells, and is active against bacterial infections. The mechanism of action for this drug is not fully understood, but it may inhibit DNA synthesis by binding to the enzyme topoisomerase II. This drug has also been shown to have analgesic effects due to its ability to block prostaglandin production in the central nervous system.

Formula: C₁₀H₁₀N₂O

Purity: Min. 95%

Molecular weight: 174.2 g/mol

Ref: 3D-HFA97343