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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)-

6-Quinolinecarboxylicacid, 2-(trifluoromethyl)-

OC(=O)c1ccc2c(c1)ccc(n2)C(F)(F)F Request for Quotation
Chemical Name: 6-Quinolinecarboxylicacid, 2-(trifluoromethyl)-
CAS Number: 952182-51-3
Product Number: AG00IIUA(AGN-PC-07A7OB)
Synonyms:
MDL No:
Molecular Formula: C11H6F3NO2
Molecular Weight: 241.1660

Identification/Properties

Computed Properties
Molecular Weight:
241.169g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
241.035g/mol
Monoisotopic Mass:
241.035g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
306
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


The application of 2-(Trifluoromethyl)quinoline-6-carboxylic acid in chemical synthesis lies in its versatility as a building block for various organic compounds. This compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals due to its unique structural features and reactivity.2-(Trifluoromethyl)quinoline-6-carboxylic acid can be utilized in the formation of heterocyclic compounds, which are essential in drug discovery and development. Its trifluoromethyl group imparts enhanced lipophilicity and metabolic stability to resulting molecules, making them potentially more effective as therapeutic agents. Additionally, the quinoline ring system offers favorable interactions with biological targets, further augmenting the compound's utility in medicinal chemistry.In synthetic organic chemistry, this acid can participate in various reactions such as nucleophilic substitution, acylation, and cyclization, leading to the formation of diverse molecular scaffolds. Its presence in the chemical toolbox enables the efficient construction of complex molecules with specific functionalities, supporting the advancement of drug design and material science.Overall, the strategic incorporation of 2-(Trifluoromethyl)quinoline-6-carboxylic acid in chemical synthesis facilitates the development of novel compounds with potential applications in pharmaceuticals, crop protection, and materials research. Its versatile nature and synthetic accessibility make it a valuable building block for the creation of diverse molecular architectures with tailored properties and biological activities.