CAS 529-37-3

4(1H)-Quinolinone

Description:

4(1H)-Quinolinone, with the CAS number 529-37-3, is a heterocyclic organic compound characterized by a fused ring structure that includes a quinoline moiety and a carbonyl group. This compound typically appears as a yellow to brown crystalline solid and is known for its aromatic properties, which contribute to its stability and reactivity. It is soluble in organic solvents such as ethanol and dimethyl sulfoxide, but has limited solubility in water. 4(1H)-Quinolinone exhibits biological activity, making it of interest in medicinal chemistry, particularly for its potential as an antimicrobial and anticancer agent. The compound can participate in various chemical reactions, including nucleophilic substitutions and cyclizations, due to the presence of the nitrogen atom in the quinoline ring. Its derivatives are often synthesized for research purposes, exploring their pharmacological properties and applications in drug development. Overall, 4(1H)-Quinolinone serves as a valuable scaffold in organic synthesis and medicinal chemistry.

Formula: C₉H₇NO

InChI: InChI=1S/C9H7NO/c11-9-5-6-10-8-4-2-1-3-7(8)9/h1-6H,(H,10,11)

InChI key: InChIKey=PMZDQRJGMBOQBF-UHFFFAOYSA-N

SMILES: O=C1C=2C(NC=C1)=CC=CC2

Synonyms:

• 1,4-Dihydro-4-quinolinone
• 1H-4-Oxoquinoline
• 1H-Quinolin-4-one
• 4(1H)-Quinolone
• 4(1H)-Quinolone(6CI,7CI,8CI)
• 4-Quinolone
• Nsc 263800
• g-Quinolone
• 4(1H)-Quinolinone

4(1H)-Quinolinone

CAS: 529-37-3

Formula: C₉H₇NO

Purity: 98%

Color and Shape: Solid

Molecular weight: 145.1580

Ref: IN-DA00D970

Quinolin-4(1H)-one

CAS: 529-37-3

Quinolin-4(1H)-one

Purity: 99%

Color and Shape: Solid

Molecular weight: 145.16g/mol

Ref: 54-OR946853

Ivacaftor Impurity 10

CAS: 529-37-3

Formula: C₉H₇NO

Molecular weight: 145.16

Ref: 4Z-I-056021

Quinolin-4(1H)-one

Controlled Product

CAS: 529-37-3

Applications Quinolin-4(1h)-one (cas# 529-37-3) is a useful research chemical.

Formula: C₉H₇NO

Color and Shape: Neat

Molecular weight: 145.16

Ref: TR-Q990023