2249-28-7 | 4-[3-(Trifluoromethyl)phenyl]-4-piperidinol

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$46.00	$32.00
250mg	95%	in stock	$56.00	$39.00
1g	95%	in stock	$79.00	$55.00
5g	95%	in stock	$231.00	$162.00
25g	95%	in stock	$667.00	$467.00
100g	95%	in stock	$2,004.00	$1,403.00

Description

• Catalog Number: AB66448
• Chemical Name: 4-[3-(Trifluoromethyl)phenyl]-4-piperidinol
• CAS Number: 2249-28-7
• Molecular Formula: C12H14F3NO
• Molecular Weight: 245.2409
• MDL Number: MFCD00044832
• SMILES: OC1(CCNCC1)c1cccc(c1)C(F)(F)F

Computed Properties

• Complexity: 261
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 1.8

Upstream Synthesis Route

4-[3-(Trifluoromethyl)phenyl]-4-piperidinol, also known as $name$, is a valuable intermediate compound widely utilized in chemical synthesis. Its unique structure containing a trifluoromethyl group attached to a phenyl ring and a piperidinol moiety makes it a versatile building block in organic chemistry.One key application of $name$ is in the synthesis of pharmaceuticals. The presence of the trifluoromethyl group can enhance the bioactivity and metabolic stability of drugs, making it an attractive substitution pattern in drug design. By using $name$ as a starting material, chemists can access a variety of drug candidates with improved pharmacological properties.Moreover, $name$ can be employed in the synthesis of agrochemicals and functional materials. The piperidinol group in its structure allows for potential interactions with biological targets, while the trifluoromethylphenyl unit can modulate the physicochemical properties of the final products. This versatility makes $name$ a valuable tool for creating novel compounds with diverse applications.In organic synthesis, the reactivity of $name$ can be fine-tuned through functional group manipulations, enabling the formation of complex molecules with high selectivity and efficiency. Chemical transformations involving $name$ can lead to the construction of intricate molecular frameworks, making it a crucial component in the toolbox of synthetic chemists.Overall, the strategic incorporation of 4-[3-(Trifluoromethyl)phenyl]-4-piperidinol in chemical synthesis enables the streamlined access to biologically active compounds, advanced materials, and structurally diverse molecules with potential pharmaceutical, agricultural, and industrial applications.