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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

5-Quinolinecarboxylic acid, ethyl ester

CCOC(=O)c1cccc2c1cccn2 Request for Quotation
Chemical Name: 5-Quinolinecarboxylic acid, ethyl ester
CAS Number: 98421-25-1
Product Number: AG00IK2Y(AGN-PC-0JP72V)
Synonyms:
MDL No:
Molecular Formula: C12H11NO2
Molecular Weight: 201.2212

Identification/Properties

Computed Properties
Molecular Weight:
201.225g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
201.079g/mol
Monoisotopic Mass:
201.079g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
230
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 5-quinolinecarboxylate, also known as ethyl quinaldate, is a versatile compound used in chemical synthesis for a wide range of applications. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and organic molecules. Its unique structure and reactivity make it a valuable intermediate in the production of diverse compounds.In chemical synthesis, ethyl 5-quinolinecarboxylate can be used as a starting material for the preparation of heterocyclic compounds, which are essential in the development of new drugs and materials. This compound can undergo various transformations, such as substitution, addition, and cyclization reactions, to yield structurally diverse products with potentially valuable properties.Ethyl 5-quinolinecarboxylate is particularly valuable in the synthesis of quinoline derivatives, which have shown promising pharmacological activities, including antimalarial, antibacterial, and anticancer properties. Additionally, this compound can be utilized in the construction of complex molecules with multiple functional groups, making it a versatile tool for organic chemists in designing novel compounds.Overall, ethyl 5-quinolinecarboxylate plays a crucial role in chemical synthesis by providing a platform for the efficient construction of biologically active molecules and functional materials. Its versatility and synthetic utility make it a valuable asset in the synthesis of diverse compounds with potential applications in various industries.