[2-(Trifluoromethyl)pyridin-4-yl]methanamine hydrochloride


Chemical Name: [2-(Trifluoromethyl)pyridin-4-yl]methanamine hydrochloride
CAS Number: 916304-20-6
Product Number: AG006FJY(AGN-PC-0WAIWA)
Synonyms:
MDL No:
Molecular Formula: C7H7F3N2
Molecular Weight: 176.1391

Identification/Properties


Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
176.142g/mol
XLogP3:
0.6
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



(2-(Trifluoromethyl)pyridin-4-yl)methanamine, commonly referred to as $name$, is a valuable chemical compound extensively utilized in chemical synthesis procedures. This compound serves as a versatile building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its functional group reactivity and unique structure.In chemical synthesis, $name$ acts as a key intermediate in the formation of complex organic molecules. Its trifluoromethyl and pyridine moieties make it a highly sought-after reagent for introducing fluorine-containing functional groups into target compounds. The trifluoromethyl group enhances the lipophilicity and metabolic stability of the final products, while the pyridine ring imparts desirable electronic properties, influencing the bioactivity of the synthesized molecules.Moreover, the amino functionality of (2-(Trifluoromethyl)pyridin-4-yl)methanamine enables it to participate in various types of chemical reactions, including nucleophilic substitution, reductive amination, and transition metal-catalyzed cross-coupling reactions. This broad reactivity profile makes $name$ a valuable tool for organic chemists seeking to construct complex molecular architectures efficiently and with high precision.Overall, the application of (2-(Trifluoromethyl)pyridin-4-yl)methanamine in chemical synthesis represents a significant advancement in the field of organic chemistry, offering researchers a powerful and versatile reagent for the development of novel compounds with potential applications in pharmaceutical, agricultural, and materials science industries.