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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-[4-(trifluoromethyl)phenyl]pyridine-2-carboxylic acid

OC(=O)c1cccc(n1)c1ccc(cc1)C(F)(F)F Request for Quotation
Chemical Name: 6-[4-(trifluoromethyl)phenyl]pyridine-2-carboxylic acid
CAS Number: 924817-68-5
Product Number: AG006HUV(AGN-PC-04Q6LJ)
Synonyms:
MDL No: MFCD06410071
Molecular Formula: C13H8F3NO2
Molecular Weight: 267.2033

Identification/Properties

Properties
Storage:
2-8℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
267.207g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
267.051g/mol
Monoisotopic Mass:
267.051g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
324
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-H320-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-(4-(Trifluoromethyl)phenyl)picolinic acid is a versatile compound commonly used in chemical synthesis as a key building block for creating pharmaceuticals, agrochemicals, and advanced materials. This compound exhibits unique properties that make it a valuable ingredient in the creation of complex organic molecules. In chemical synthesis, 6-(4-(Trifluoromethyl)phenyl)picolinic acid serves as a valuable starting material for the incorporation of trifluoromethyl groups into various organic compounds, enhancing their stability, lipophilicity, and biological activity. Additionally, this compound can be utilized in the preparation of chiral ligands for asymmetric catalysis, as well as in the synthesis of fluorescent probes for biological imaging applications. Its versatility and reactivity make it an indispensable tool for chemists working in the field of organic chemistry and drug discovery.