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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)-

4-Quinolinecarboxylic acid, 2-(2-fluorophenyl)-

Fc1ccccc1c1nc2ccccc2c(c1)C(=O)O Request for Quotation
Chemical Name: 4-Quinolinecarboxylic acid, 2-(2-fluorophenyl)-
CAS Number: 1647-89-8
Product Number: AG001V1Z(AGN-PC-0KL277)
Synonyms:
MDL No:
Molecular Formula: C16H10FNO2
Molecular Weight: 267.2545

Identification/Properties

Properties
MP:
230 °C
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
267.259g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
267.07g/mol
Monoisotopic Mass:
267.07g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
362
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(2-Fluorophenyl)quinoline-4-carboxylic acid is a versatile compound commonly utilized in chemical synthesis for a variety of applications. In organic chemistry, this compound serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and functional groups make it a valuable intermediate in the synthesis of complex organic molecules.This compound can undergo diverse chemical transformations, such as derivatization, reduction, oxidation, and coupling reactions, to generate new compounds with desired properties. By functionalizing the quinoline core and the carboxylic acid moiety, chemists can modulate the chemical and pharmacological properties of the resulting compounds.In pharmaceutical synthesis, 2-(2-Fluorophenyl)quinoline-4-carboxylic acid may be used to create potential drug candidates targeting specific biological pathways or diseases. Its presence in the molecular structure can influence the compound's pharmacokinetic profile, binding affinity, and metabolic stability.Furthermore, in agrochemical synthesis, this compound can be incorporated into the design of novel pesticides, herbicides, or fungicides with improved efficacy and environmental safety. Its use in chemical synthesis extends to material science, where it can be employed to develop functional materials, dyes, or catalysts with enhanced performance.Overall, the application of 2-(2-Fluorophenyl)quinoline-4-carboxylic acid in chemical synthesis enables chemists to access a diverse range of compounds with potential industrial, pharmaceutical, and agricultural applications.