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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)-

2-Quinolinecarboxylic acid, 8-hydroxy-, ethyl ester

CCOC(=O)c1ccc2c(n1)c(O)ccc2 Request for Quotation
Chemical Name: 2-Quinolinecarboxylic acid, 8-hydroxy-, ethyl ester
CAS Number: 138085-04-8
Product Number: AG0017ZG(AGN-PC-0J0Y73)
Synonyms:
MDL No:
Molecular Formula: C12H11NO3
Molecular Weight: 217.2206

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 8-hydroxyquinoline-2-carboxylate is often utilized in chemical synthesis as a key building block for the preparation of various organic compounds. Its unique structure and functional groups make it a versatile compound with multiple applications in the field of organic chemistry.One common application of Ethyl 8-hydroxyquinoline-2-carboxylate is in the synthesis of heterocyclic compounds. Its quinoline ring provides a valuable scaffold for the construction of complex molecules with diverse biological activities. By utilizing Ethyl 8-hydroxyquinoline-2-carboxylate as a starting material, chemists can introduce different functional groups and modifications to the quinoline structure, leading to the creation of novel compounds for pharmaceutical or material science purposes.Additionally, Ethyl 8-hydroxyquinoline-2-carboxylate can also serve as a ligand in coordination chemistry. Due to the presence of the hydroxy and carboxylate groups, it can form coordination complexes with metal ions, offering a wide range of applications in catalysis, material synthesis, and coordination chemistry studies.Overall, the use of Ethyl 8-hydroxyquinoline-2-carboxylate in chemical synthesis enables chemists to access a diverse array of organic compounds with unique properties and applications in various fields of chemistry.