Molecular properties
- Formula
- C19H15ClN2O4
- Molar mass
- 370.79 g·mol−1
- Exact mass
- 370.0720 Da
- 13
- PubChem CID
- 5042
Molecule record
2-[(4-chlorobenzoyl)amino]-3-(2-oxo-1H-quinolin-4-yl)propanoic acid
C19H15ClN2O4
370.79 g/mol
Loading structure
Functional groups
Alkane / alkyl carbon
Amide
Aromatic ring
Aryl halide
Carboxylic acid
Secondary amine
Physical properties
No source-backed physical properties are curated for this molecule yet.
Common names and synonyms
- (2RS)-2-(4-Chlorobenzoylamino)-3-(2-oxo-1,2-dihydroquinolin-4-yl)propanoic acid
- 111911-87-6
- 139344-42-6
- 2-(4-Chlorobenzoylamino)-3-(1,2-dihydro-2-oxo-4-quinolyl)propionic acid
- 2-(4-chlorobenzoylamino)-3-(2(1H)-quinolinon-4-yl)propionic acid
- 2-[(4-chlorophenyl)formamido]-3-(2-oxo-1,2-dihydroquinolin-4-yl)propanoic acid
- 815-380-0
- 90098-04-7
Show all 24 synonyms
- A02BX14
- DTXCID6025937
- DTXSID8045937
- LR583V32ZR
- MFCD00866895
- Mucosta
- NSC-758955
- OPC-12759
- Pramipide
- Proamipide
- Rebamipida
- Rebamipidum
- Rebator
- RefChem:878997
- alpha-((4-Chlorobenzoyl)amino)-1,2-dihydro-2-oxo-4-quinolinepropanoic Acid
- rebamipide
Structure identifiers
- Canonical SMILES
- O=C(NC(Cc1cc(=O)[nH]c2ccccc12)C(=O)O)c1ccc(Cl)cc1
- Isomeric SMILES
- C1=CC=C2C(=C1)C(=CC(=O)N2)CC(C(=O)O)NC(=O)C3=CC=C(C=C3)Cl
- InChI
- InChI=1S/C19H15ClN2O4/c20-13-7-5-11(6-8-13)18(24)22-16(19(25)26)9-12-10-17(23)21-15-4-2-1-3-14(12)15/h1-8,10,16H,9H2,(H,21,23)(H,22,24)(H,25,26)
- InChIKey
- ALLWOAVDORUJLA-UHFFFAOYSA-N
- PubChem CID
- 5042
Spectroscopy
Tabs appear only for spectra stored with clear provenance.
No redistributable or simulated spectroscopy record is attached yet.
Simulated NMR
On-demand educational prediction for 2-[(4-chlorobenzoyl)amino]-3-(2-oxo-1H-quinolin-4-yl)propanoic acid; not experimental data.
Simulated EI mass spectrum
On-demand educational fragmentation for 2-[(4-chlorobenzoyl)amino]-3-(2-oxo-1H-quinolin-4-yl)propanoic acid; not experimental data.
Sources
Molecule identity
Retrieved 8/20/2026. Reuse status is summarized by the badge; open the source for full details.