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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)-

ethyl 1-ethyl-6,7,8-trifluoro-4-oxoquinoline-3-carboxylate

CCOC(=O)c1cn(CC)c2c(c1=O)cc(c(c2F)F)F Request for Quotation
Chemical Name: ethyl 1-ethyl-6,7,8-trifluoro-4-oxoquinoline-3-carboxylate
CAS Number: 100501-62-0
Product Number: AG000263(AGN-PC-0LNBVE)
Synonyms:
MDL No:
Molecular Formula: C14H12F3NO3
Molecular Weight: 299.2452

Identification/Properties

Properties
MP:
204-208 °C
BP:
392.3 °C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
299.249g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
4
Exact Mass:
299.077g/mol
Monoisotopic Mass:
299.077g/mol
Topological Polar Surface Area:
46.6A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
468
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 1-ethyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate is a versatile compound widely utilized in chemical synthesis as a key building block. This compound plays a crucial role in the creation of various complex organic molecules due to its unique structure and reactive properties.In chemical synthesis, Ethyl 1-ethyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate serves as a valuable starting material for the preparation of structurally diverse compounds. Its trifluoro-substituted quinoline core provides a platform for the introduction of different functional groups through various reaction pathways.By strategically modifying the carboxylate group or the ethyl side chain, chemists can tailor the properties of the final products for specific applications. This compound enables the synthesis of bioactive molecules, pharmaceutical intermediates, agrochemicals, and materials with customized functionalities.The incorporation of Ethyl 1-ethyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate in chemical reactions allows for the construction of complex molecular structures with high precision and efficiency. Its presence in the synthesis process enhances the diversity and complexity of the generated compounds, making it a valuable tool for synthetic chemists in designing novel molecules for various industrial and research purposes.