373603-69-1 | 4-(Trifluoromethyl)piperidin-4-ol

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$79.00	$56.00
5g	97%	in stock	$287.00	$201.00
10g	97%	in stock	$378.00	$265.00

Description

• Catalog Number: AF68632
• Chemical Name: 4-(Trifluoromethyl)piperidin-4-ol
• CAS Number: 373603-69-1
• Molecular Formula: C6H10F3NO
• Molecular Weight: 169.1449
• MDL Number: MFCD13179174
• SMILES: FC(C1(O)CCNCC1)(F)F

Computed Properties

• Complexity: 139
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• XLogP3: 0.6

Upstream Synthesis Route

4-(Trifluoromethyl)piperidin-4-ol, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role as a building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique chemical structure containing a trifluoromethyl group and a piperidin-4-ol moiety provides opportunities for diverse functionalization and reaction pathways.In chemical synthesis, 4-(Trifluoromethyl)piperidin-4-ol serves as a key intermediate in the production of complex molecules due to its reactivity and stability. The trifluoromethyl group can act as a directing group in transition metal-catalyzed reactions, enabling selective functionalization at specific positions within the molecule. Additionally, the piperidin-4-ol motif imparts unique steric and electronic properties that influence the overall reactivity and selectivity of the compound in various reactions.Furthermore, 4-(Trifluoromethyl)piperidin-4-ol can be utilized for the construction of chiral compounds through asymmetric synthesis strategies. Its chiral center provides an opportunity for the development of enantioselective transformations, leading to the production of enantiopure molecules with significant biological activity.Overall, the application of 4-(Trifluoromethyl)piperidin-4-ol in chemical synthesis offers a wide range of possibilities for the efficient and selective construction of complex molecular structures with diverse functionalities and stereochemistries.