50650-59-4 | 4-(Trifluoromethyl)-1H-pyridin-2-one

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$9.00	$7.00
5g	98%	in stock	$24.00	$17.00
10g	98%	in stock	$44.00	$31.00
25g	98%	in stock	$90.00	$63.00

Description

• Catalog Number: AB62311
• Chemical Name: 4-(Trifluoromethyl)-1H-pyridin-2-one
• CAS Number: 50650-59-4
• Molecular Formula: C6H4F3NO
• Molecular Weight: 163.0973
• MDL Number: MFCD00153195
• SMILES: Oc1nccc(c1)C(F)(F)F

Computed Properties

• Complexity: 239
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• XLogP3: 0.6

Upstream Synthesis Route

4-(Trifluoromethyl)pyridin-2-ol plays a crucial role in chemical synthesis as a versatile building block and intermediate. Its unique structure and chemical properties make it a valuable component in the development of various compounds across the pharmaceutical, agrochemical, and material science industries. In chemical synthesis, 4-(Trifluoromethyl)pyridin-2-ol can be utilized as a key starting material for the preparation of complex molecules through multi-step synthetic routes. Its trifluoromethyl group provides enhanced lipophilicity and electron-withdrawing properties, which are essential for modulating the biological activity and physicochemical properties of the final products.This compound is particularly valuable in the synthesis of pharmaceutical compounds due to its ability to impart desirable pharmacokinetic and pharmacodynamic profiles. Additionally, 4-(Trifluoromethyl)pyridin-2-ol can serve as a valuable precursor in the preparation of fluorinated building blocks, which are in high demand for the development of novel drug candidates with improved metabolic stability and target specificity.Furthermore, the presence of both a pyridine and a hydroxyl group in 4-(Trifluoromethyl)pyridin-2-ol offers opportunities for further functionalization through various chemical transformations, enabling the synthesis of a diverse array of compounds with tailored properties. Its versatility and compatibility with different synthetic methodologies make it an indispensable tool for organic chemists working on the design and synthesis of biologically active molecules and advanced materials.