CAS 1416440-22-6
:Ethyl 5-amino-3-quinolinecarboxylate
Description:
Ethyl 5-amino-3-quinolinecarboxylate is a chemical compound characterized by its quinoline structure, which is a bicyclic aromatic compound containing a nitrogen atom in the ring. This substance features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of an amino group at the 5-position of the quinoline ring enhances its potential for various chemical reactions, including nucleophilic substitutions and coupling reactions. Ethyl 5-amino-3-quinolinecarboxylate is typically used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its properties, such as melting point, boiling point, and solubility, can vary based on the specific conditions and purity of the compound. Additionally, the compound's reactivity can be influenced by the electronic effects of the amino and carboxylate groups, making it a valuable building block in medicinal chemistry and material science. Safety data should be consulted for handling and storage, as with any chemical substance.
Formula:C12H12N2O2
InChI:InChI=1S/C12H12N2O2/c1-2-16-12(15)8-6-9-10(13)4-3-5-11(9)14-7-8/h3-7H,2,13H2,1H3
InChI key:InChIKey=CRHQHVDNHKUISX-UHFFFAOYSA-N
SMILES:NC=1C2=C(N=CC(C(OCC)=O)=C2)C=CC1
Synonyms:- 3-Quinolinecarboxylic acid, 5-amino-, ethyl ester
- Ethyl 5-amino-3-quinolinecarboxylate
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
3-Quinolinecarboxylic acid, 5-amino-, ethyl ester
CAS:Formula:C12H12N2O2Purity:98%Color and Shape:SolidMolecular weight:216.2359Ethyl 5-aminoquinoline-3-carboxylate
CAS:<p>Ethyl 5-aminoquinoline-3-carboxylate</p>Purity:98%Molecular weight:216.24g/molETHYL 5-AMINOQUINOLINE-3-CARBOXYLATE
CAS:Formula:C12H12N2O2Purity:95.0%Color and Shape:SolidMolecular weight:216.24



