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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-Pyridinamine, 5-(trifluoromethyl)-

FC(c1cncc(c1)N)(F)F Request for Quotation
Chemical Name: 3-Pyridinamine, 5-(trifluoromethyl)-
CAS Number: 112110-07-3
Product Number: AG007CEE(AGN-PC-0009AT)
Synonyms:
MDL No:
Molecular Formula: C6H5F3N2
Molecular Weight: 162.1125

Identification/Properties

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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(Trifluoromethyl)pyridin-3-amine is a versatile compound that finds extensive application in chemical synthesis. With its unique structure and properties, this chemical plays a crucial role in various organic reactions and transformations. Its trifluoromethyl group imparts important characteristics to the molecule, enhancing its reactivity and influencing the outcomes of reactions it participates in. The presence of the pyridine ring further expands its utility, allowing for the formation of diverse chemical compounds.In organic synthesis, 5-(Trifluoromethyl)pyridin-3-amine serves as a valuable building block for the construction of complex molecules and functional materials. Its use can lead to the synthesis of pharmaceuticals, agrochemicals, and advanced materials with enhanced properties. The amine functional group in the molecule also enables it to participate in a wide range of reactions, further increasing its synthetic versatility.Overall, the application of 5-(Trifluoromethyl)pyridin-3-amine in chemical synthesis enables chemists to access novel compounds and derivatives with potential applications across various industries, making it a valuable tool in modern organic chemistry.