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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-Pyridinamine, 2-(trifluoromethyl)-

FC(c1nccc(c1)N)(F)F Request for Quotation
Chemical Name: 4-Pyridinamine, 2-(trifluoromethyl)-
CAS Number: 147149-98-2
Product Number: AG001EO4(AGN-PC-0N1IA3)
Synonyms:
MDL No: MFCD09056877
Molecular Formula: C6H5F3N2
Molecular Weight: 162.1125

Identification/Properties

Properties
MP:
58-62°C
BP:
230.7°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
162.115g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
162.04g/mol
Monoisotopic Mass:
162.04g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
134
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


4-Amino-2-(trifluoromethyl)pyridine is a versatile compound widely utilized in chemical synthesis for its unique properties. This compound serves as a valuable building block in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its trifluoromethyl group enhances the compound's reactivity and stability, making it a highly sought-after reagent in organic synthesis.In chemical synthesis, 4-Amino-2-(trifluoromethyl)pyridine can act as a nucleophilic reagent, participating in various substitution reactions to introduce the trifluoromethyl group into organic molecules. This compound is particularly valuable in medicinal chemistry for the incorporation of the trifluoromethyl moiety, as it can enhance the biological activity and metabolic stability of drug candidates.Additionally, 4-Amino-2-(trifluoromethyl)pyridine can serve as a key intermediate in the synthesis of fluorinated heterocycles, which are essential structural motifs found in many biologically active compounds. Its ability to undergo diverse transformations, such as cross-coupling reactions and functional group manipulations, makes it a valuable tool for building complex molecular architectures in chemical synthesis.Overall, the application of 4-Amino-2-(trifluoromethyl)pyridine in chemical synthesis extends to a wide range of industries, including pharmaceuticals, agrochemicals, and materials science, where its unique properties and versatility contribute to the development of innovative products and processes.