CAS 142326-59-8
:7-Chloro-4-hydroxy-3-(3-phenoxyphenyl)-2(1H)-quinolinone
Description:
7-Chloro-4-hydroxy-3-(3-phenoxyphenyl)-2(1H)-quinolinone, with the CAS number 142326-59-8, is a synthetic organic compound characterized by its quinolinone core structure, which is a bicyclic compound featuring a fused benzene and pyridine ring. This compound exhibits a chloro substituent at the 7-position and a hydroxy group at the 4-position, contributing to its potential biological activity. The presence of a phenoxyphenyl group at the 3-position enhances its lipophilicity and may influence its interaction with biological targets. Typically, compounds of this class are investigated for their pharmacological properties, including antimicrobial and anticancer activities. The molecular structure suggests that it may participate in hydrogen bonding due to the hydroxyl group, which could affect its solubility and reactivity. Additionally, the chlorine atom may influence the electronic properties of the molecule, potentially enhancing its biological efficacy. Overall, this compound represents a class of heterocyclic compounds with diverse applications in medicinal chemistry.
Formula:C21H14ClNO3
InChI:InChI=1S/C21H14ClNO3/c22-14-9-10-17-18(12-14)23-21(25)19(20(17)24)13-5-4-8-16(11-13)26-15-6-2-1-3-7-15/h1-12H,(H2,23,24,25)
InChI key:InChIKey=FLVRDMUHUXVRET-UHFFFAOYSA-N
SMILES:OC1=C(C2=CC(OC3=CC=CC=C3)=CC=C2)C(=O)NC=4C1=CC=C(Cl)C4
Synonyms:- L 701324
- 7-Chloro-4-hydroxy-3-(3-phenoxyphenyl)-2(1H)-quinolinone
- 2(1H)-Quinolinone, 7-chloro-4-hydroxy-3-(3-phenoxyphenyl)-
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Found 7 products.
7-Chloro-4-Hydroxy-3-(3-Phenoxyphenyl)Quinolin-2(1H)-One
CAS:7-Chloro-4-Hydroxy-3-(3-Phenoxyphenyl)Quinolin-2(1H)-OnePurity:98%Molecular weight:363.79g/molL-701324
CAS:<p>L-701324 is an NMDA receptor with high affinity and selectivity for the glycine site, used as an orally active and long-acting anticonvulsant.</p>Formula:C21H14ClNO3Purity:98.63% - >99.99%Color and Shape:SolidMolecular weight:363.79L-701,324
CAS:<p>L-701,324 is a selective antagonist of the response element-binding protein (REB). It prevents the transcription of the gene encoding this protein by binding to its DNA-binding site in the regulatory region of this gene. L-701,324 has been shown to have antagonistic effects on glutamate receptors and may be useful for treating neurodegenerative disorders. L-701,324 has also been shown to have anti-locomotor activity in animals and an interactive effect with other pharmacological agents. This drug has not yet been evaluated in humans.</p>Formula:C21H14ClNO3Purity:Min. 95%Molecular weight:363.79 g/mol





