37885-07-7 | 1-(2-Amino-4-(trifluoromethyl)phenyl)ethanone

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$20.00	$14.00
1g	98%	in stock	$79.00	$56.00
5g	98%	in stock	$394.00	$276.00

Description

• Catalog Number: AB56372
• Chemical Name: 1-(2-Amino-4-(trifluoromethyl)phenyl)ethanone
• CAS Number: 37885-07-7
• Molecular Formula: C9H8F3NO
• Molecular Weight: 203.1611
• MDL Number: MFCD11113374
• SMILES: CC(=O)c1ccc(cc1N)C(F)(F)F

Computed Properties

• Complexity: 227
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.4

Upstream Synthesis Route

1-(2-Amino-4-(trifluoromethyl)phenyl)ethanone, commonly referred to as $name$, is a versatile chemical compound that plays a significant role in chemical synthesis. This compound is utilized in a variety of chemical reactions and processes to introduce the amino and trifluoromethyl functional groups into target molecules. In chemical synthesis, $name$ serves as a key building block for the preparation of various pharmaceuticals, agrochemicals, and advanced materials. Its unique structure containing both an amino group and a trifluoromethyl group make it a valuable intermediate for the synthesis of complex organic molecules. $name$ is particularly valuable in medicinal chemistry, where the introduction of the trifluoromethyl group can significantly influence the biological activity and properties of the resulting compounds. This compound is often used in the development of pharmaceuticals with enhanced efficacy and improved pharmacokinetic profiles. Furthermore, $name$ finds applications in the synthesis of fluorinated organic compounds, which are of great interest in medicinal chemistry, materials science, and other fields. The trifluoromethyl group in $name$ can serve as a versatile handle for further functionalization, allowing for the creation of a wide range of fluorinated molecules with unique properties. Overall, the application of 1-(2-Amino-4-(trifluoromethyl)phenyl)ethanone in chemical synthesis enables chemists to access a diverse array of functionalized compounds with important implications in drug discovery, materials science, and other areas of research.