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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-Pyridinecarboxylic acid, 6-[4-(trifluoromethoxy)phenyl]-

OC(=O)c1ccc(nc1)c1ccc(cc1)OC(F)(F)F Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 6-[4-(trifluoromethoxy)phenyl]-
CAS Number: 851266-74-5
Product Number: AG00G2UJ(AGN-PC-04Q6I0)
Synonyms:
MDL No: MFCD06410408
Molecular Formula: C13H8F3NO3
Molecular Weight: 283.2027296

Identification/Properties

Computed Properties
Molecular Weight:
283.206g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
3
Exact Mass:
283.046g/mol
Monoisotopic Mass:
283.046g/mol
Topological Polar Surface Area:
59.4A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
340
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


6-(4-(Trifluoromethoxy)phenyl)nicotinic acid is a versatile compound commonly utilized in chemical synthesis for its unique properties. This acid serves as a valuable building block in organic chemistry, particularly in the synthesis of pharmaceutical intermediates and agrochemicals. Its trifluoromethoxyphenyl group imparts enhanced reactivity and selectivity to reactions, making it a valuable tool for the creation of complex molecular structures. This compound is frequently employed in the development of novel drug candidates and fine chemicals due to its ability to modulate biological activity and optimize properties. In chemical synthesis, 6-(4-(Trifluoromethoxy)phenyl)nicotinic acid plays a crucial role in facilitating the construction of diverse molecular architectures with specific functionalities, making it an indispensable component in the toolbox of synthetic chemists.