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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-(trifluoromethyl)pyridin-2-yl]methanamine

NCc1cccc(n1)C(F)(F)F Request for Quotation
Chemical Name: [6-(trifluoromethyl)pyridin-2-yl]methanamine
CAS Number: 916304-19-3
Product Number: AG006RK9(AGN-PC-0KZ49D)
Synonyms:
MDL No:
Molecular Formula: C7H7F3N2
Molecular Weight: 176.1391

Identification/Properties

Properties
BP:
177.8±35.0°C at 760mmHg
Storage:
2-8℃;Light sensitive;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
176.142g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
176.056g/mol
Monoisotopic Mass:
176.056g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
146
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(6-(Trifluoromethyl)pyridin-2-yl)methanamine is a versatile compound that plays a crucial role in chemical synthesis. Its primary application lies in its function as a valuable building block in organic chemistry reactions, particularly in medicinal chemistry and pharmaceutical research. This compound serves as a key intermediate in the synthesis of various biologically active molecules, including potential drug candidates and agrochemicals.The trifluoromethyl group attached to the pyridine ring confers unique properties to this compound, enhancing its reactivity and allowing for the introduction of fluorine atoms into target molecules. The presence of the amino group further expands the compound's utility by enabling the formation of important amide, imine, or reductive amination products. Additionally, the pyridine ring itself can participate in diverse cross-coupling reactions, facilitating the creation of complex molecular structures.In summary, (6-(Trifluoromethyl)pyridin-2-yl)methanamine serves as a valuable synthetic tool for chemists working in the fields of drug discovery, agrochemical development, and materials science. Its strategic incorporation into synthetic routes enables the efficient and selective construction of novel compounds with potential applications across various industries.