Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H9NO |
| Molecular Weight | 147.1739 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1CCC2=CC=CC=C2N1
InChI
InChIKey=TZOYXRMEFDYWDQ-UHFFFAOYSA-N
InChI=1S/C9H9NO/c11-9-6-5-7-3-1-2-4-8(7)10-9/h1-4H,5-6H2,(H,10,11)
| Molecular Formula | C9H9NO |
| Molecular Weight | 147.1739 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis of 3-methoxycarbonylmethyl derivatives of dihydroquinolone and dihydrochromenone. | 2001 Mar 23 |
|
| Quinoline and derivatives at a tar oil contaminated site: hydroxylated products as indicator for natural attenuation? | 2007 Aug 1 |
|
| In vivo active aldosterone synthase inhibitors with improved selectivity: lead optimization providing a series of pyridine substituted 3,4-dihydro-1H-quinolin-2-one derivatives. | 2008 Dec 25 |
|
| Synthesis and biological activity of quinolinone and dihydroquinolinone p38 MAP kinase inhibitors. | 2008 Mar 15 |
|
| Novel approach to 3,4-dihydro-2(1H)-quinolinone derivatives via cyclopropane ring expansion. | 2009 Mar 5 |
|
| Ethyl 6-chloro-2-oxo-4-phenyl-1,2-dihydro-quinoline-3-carboxyl-ate. | 2009 Nov 4 |
|
| Synthesis of highly enantioenriched 3,4-dihydroquinolin-2-ones by 6-exo-trig radical cyclizations of axially chiral alpha-halo-ortho-alkenyl anilides. | 2009 Oct 28 |
|
| (RS)-3-Acetyl-2-methyl-4-(3-nitro-phen-yl)-1,4,5,6,7,8-hexa-hydro-quinolin-5-one. | 2009 Sep 26 |
|
| Potent dihydroquinolinone dopamine D2 partial agonist/serotonin reuptake inhibitors for the treatment of schizophrenia. | 2010 May 1 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 04:29:10 GMT 2023
by
admin
on
Sat Dec 16 04:29:10 GMT 2023
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| Record UNII |
2CKG6TX32F
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| Record Status |
Validated (UNII)
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| Record Version |
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