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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)-

3-Quinolinecarboxylic acid, 4-hydroxy-8-(trifluoromethyl)-, ethyl ester

CCOC(=O)c1cnc2c(c1O)cccc2C(F)(F)F Request for Quotation
Chemical Name: 3-Quinolinecarboxylic acid, 4-hydroxy-8-(trifluoromethyl)-, ethyl ester
CAS Number: 23851-84-5
Product Number: AG003QAZ(AGN-PC-0O84P3)
Synonyms:
MDL No: MFCD00173387
Molecular Formula: C13H10F3NO3
Molecular Weight: 285.2186

Identification/Properties

Properties
BP:
271.4°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
285.222g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
3
Exact Mass:
285.061g/mol
Monoisotopic Mass:
285.061g/mol
Topological Polar Surface Area:
55.4A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
445
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 4-hydroxy-8-(trifluoromethyl)quinoline-3-carboxylate is a versatile compound widely used in chemical synthesis, particularly in the field of medicinal chemistry. This organic compound serves as a key building block in the creation of various pharmaceutical agents and functional materials. Its unique structure containing a quinoline ring with a hydroxy group and a trifluoromethyl substituent provides opportunities for diverse chemical reactions and transformations.One notable application of Ethyl 4-hydroxy-8-(trifluoromethyl)quinoline-3-carboxylate in chemical synthesis is its role as a precursor in the development of novel drug candidates. By incorporating this compound into the molecular structure of potential pharmaceuticals, researchers can explore its effects on biological targets and optimize the properties of the final drug molecules. Additionally, the presence of the trifluoromethyl group offers advantages in terms of enhancing the biological activity, metabolic stability, and pharmacokinetic profile of the resulting drugs.Furthermore, Ethyl 4-hydroxy-8-(trifluoromethyl)quinoline-3-carboxylate can also be utilized in the synthesis of advanced materials with specialized functions. Its ability to participate in various synthetic transformations allows for the creation of customized materials for applications in fields such as organic electronics, catalysis, and materials science. By incorporating this compound into the design of molecular systems, researchers can tailor the properties of the materials for specific technological purposes, opening up new avenues for innovation and discovery in material science.