1227581-75-0 | 2-Amino-4-(trifluoromethyl)pyridin-3-ol

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	2 weeks	$1,858.00	$1,300.00
5g	95%	2 weeks	$3,643.00	$2,550.00

Description

• Catalog Number: BC48586
• Chemical Name: 2-Amino-4-(trifluoromethyl)pyridin-3-ol
• CAS Number: 1227581-75-0
• Molecular Formula: C6H5F3N2O
• Molecular Weight: 178.1119
• MDL Number: MFCD05861552
• SMILES: Nc1nccc(c1O)C(F)(F)F

Upstream Synthesis Route

2-Amino-4-(trifluoromethyl)-3-pyridinol, or $name$, is a key reagent widely utilized in chemical synthesis due to its versatile functional groups and unique reactivity. In the realm of organic chemistry, this compound serves as a valuable building block for the construction of various complex molecules. Its trifluoromethyl group imparts significant electron-withdrawing properties and steric effects, making it a valuable tool in the design of pharmaceuticals, agrochemicals, and materials.One prominent application of 2-Amino-4-(trifluoromethyl)-3-pyridinol lies in its role as a precursor for the synthesis of fluorinated heterocycles. The presence of the trifluoromethyl group enables efficient C-F bond formation, allowing for the introduction of fluorine atoms into organic frameworks. This fluorine substitution can dramatically influence the physicochemical properties of the resulting compounds, leading to enhanced biological activity or improved material characteristics.Furthermore, the amino and hydroxyl functional groups present in 2-Amino-4-(trifluoromethyl)-3-pyridinol offer additional synthetic possibilities. These moieties can participate in a variety of chemical transformations, including nucleophilic substitution, acylation, and metal-catalyzed coupling reactions. By leveraging these diverse reactivity profiles, chemists can access structurally intricate molecules with tailored properties for specific applications.Overall, the strategic incorporation of 2-Amino-4-(trifluoromethyl)-3-pyridinol in chemical synthesis facilitates the construction of complex molecular structures with fluorine-containing motifs, highlighting its significance in the development of novel compounds with diverse functionalities.