111991-14-1 | Oxirane, [4-(trifluoromethyl)phenyl]-

Packsize	Purity	Availability	Price	Discounted Price
50mg	95%	1 week	$265.00	$185.00
100mg	95%	1 week	$354.00	$248.00
250mg	95%	1 week	$470.00	$329.00
500mg	95%	1 week	$695.00	$486.00
1g	95%	1 week	$866.00	$607.00
2.5g	95%	1 week	$1,398.00	$979.00
5g	95%	1 week	$2,280.00	$1,596.00

Description

• Catalog Number: AD43181
• Chemical Name: Oxirane, [4-(trifluoromethyl)phenyl]-
• CAS Number: 111991-14-1
• Molecular Formula: C9H7F3O
• Molecular Weight: 188.1465
• MDL Number: MFCD09950047
• SMILES: FC(c1ccc(cc1)C1OC1)(F)F

Upstream Synthesis Route

2-[4-(Trifluoromethyl)phenyl]oxirane, also known as $name$, is a highly versatile compound that finds numerous applications in chemical synthesis. Its unique molecular structure, featuring a trifluoromethyl group attached to a phenyl ring within an oxirane ring, imparts distinct properties that are valuable in the creation of various organic molecules.In chemical synthesis, $name$ is commonly utilized as a building block or reagent in the formation of complex molecules. The presence of the trifluoromethyl group enhances the compound's reactivity and stability, allowing for efficient and selective reactions. This makes it particularly useful in the synthesis of pharmaceuticals, agrochemicals, and materials with advanced functionalities.One key application of 2-[4-(Trifluoromethyl)phenyl]oxirane is in the synthesis of biologically active compounds, where the trifluoromethyl group can modulate the compound's pharmacokinetic properties and interactions with biological targets. Additionally, its oxirane ring can participate in various ring-opening reactions to introduce new functionalities or to create chiral centers, essential in the preparation of enantiomerically pure compounds.Furthermore, the presence of the phenyl ring in $name$ provides a platform for further functionalization through aromatic chemistry, enabling the synthesis of diverse derivatives with tailored properties. Its compatibility with a range of reaction conditions and ability to participate in various transformations make it a valuable tool for synthetic chemists seeking to construct complex molecular architectures efficiently and with precision.