CAS 15733-83-2: 4-methoxy-2-quinolinecarboxylic acid
Formula:C11H9NO3
InChI:InChI=1S/C11H9NO3/c1-15-10-6-9(11(13)14)12-8-5-3-2-4-7(8)10/h2-6H,1H3,(H,13,14)
InChI key:InChIKey=AVBKMSSLAIKOGM-UHFFFAOYSA-N
SMILES:O(C)C=1C2=C(N=C(C(O)=O)C1)C=CC=C2
Synonyms:- 2-Carboxy-4-methoxyquinoline
- 2-Quinolinecarboxylic acid, 4-methoxy-
- 4-Methoxyquinoline-2-Carboxylic Acid
- Quinaldic acid, 4-methoxy-
- 4-Methoxy-2-quinolinecarboxylic acid
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Found 5 products.
4-Methoxyquinoline-2-carboxylic acid
CAS:4-Methoxyquinoline-2-carboxylic acidPurity:95%Molecular weight:203.19g/mol4-Methoxy-2-quinolinecarboxylic acid
CAS:Formula:C11H9NO3Purity:≥ 97.0%Color and Shape:SolidMolecular weight:203.204-Methoxyquinoline-2-carboxylic acid
CAS:Purity:97.0%Color and Shape:SolidMolecular weight:203.197006225585944-Methoxy-2-quinolinecarboxylic acid
CAS:4-Methoxy-2-quinolinecarboxylic acid is a compound that contains a phenyl ring with two substituents, one of which is a methoxy group. It has been shown to regenerate primary alcohols from the corresponding hydroxyaldehyde under mild conditions. 4-Methoxy-2-quinolinecarboxylic acid also reacts with aldehydes to form an oxime and an acetal in the presence of base. The functional theory proposes that the molecular orbitals are formed by the overlap of atomic orbitals and may be used to explain reactions such as these. The neurotoxic effect of 4-methoxy-2-quinolinecarboxylic acid has been observed in rats after intraperitoneal injection. This compound also has been shown to catalyze the formation of bidentate ligands and chelate ligands.Formula:C11H9NO3Purity:Min. 95%Molecular weight:203.19 g/mol2-Quinolinecarboxylic acid, 4-methoxy-
CAS:Formula:C11H9NO3Purity:97%Color and Shape:SolidMolecular weight:203.1941
