(1S)-2,2,2-trifluoro-1-pyridin-3-ylethanamine


Chemical Name: (1S)-2,2,2-trifluoro-1-pyridin-3-ylethanamine
CAS Number: 912761-24-1
Product Number: AG00GS6M(AGN-PC-0566YI)
Synonyms:
MDL No:
Molecular Formula: C7H7F3N2
Molecular Weight: 176.1391

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301-H315-H319-H335
Precautionary Statements:
P261-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:

NMR Spectrum


Other Analytical Data


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Chemical Structure



2,2,2-Trifluoro-1-(pyridin-3-yl)ethanamine is a versatile compound that finds a wide range of applications in chemical synthesis. Due to its unique structure and properties, this compound is commonly utilized as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. One of the key applications of 2,2,2-Trifluoro-1-(pyridin-3-yl)ethanamine in chemical synthesis is its use as a precursor in the preparation of fluorinated organic molecules. The trifluoromethyl group present in the compound imparts valuable physicochemical properties to the target molecules, making them highly desirable in drug discovery and material science. Additionally, the amino group in 2,2,2-Trifluoro-1-(pyridin-3-yl)ethanamine enables further functionalization through various organic reactions such as reductive amination, amide formation, and cross-coupling reactions. This functional group allows for the introduction of different functionalities into the molecule, leading to the synthesis of diverse chemical compounds with tailored properties.Overall, the strategic incorporation of 2,2,2-Trifluoro-1-(pyridin-3-yl)ethanamine in chemical synthesis facilitates the development of novel molecules with enhanced biological activity, improved stability, and increased selectivity, making it a valuable tool in the pharmaceutical and agrochemical industries.