10055-40-0 | (4-Aminophenyl)(4-fluorophenyl)methanone

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$163.00	$114.00
5g	97%	in stock	$457.00	$320.00
10g	97%	in stock	$775.00	$543.00
25g	97%	in stock	$1,536.00	$1,075.00

Description

• Catalog Number: AA02802
• Chemical Name: (4-Aminophenyl)(4-fluorophenyl)methanone
• CAS Number: 10055-40-0
• Molecular Formula: C13H10FNO
• Molecular Weight: 215.223
• MDL Number: MFCD00498555
• SMILES: Nc1ccc(cc1)C(=O)c1ccc(cc1)F

Upstream Synthesis Route

(4-Aminophenyl)(4-fluorophenyl)methanone, also known as $name$, serves as a valuable building block in chemical synthesis due to its versatile reactivity and functional properties. Its application in organic chemistry encompasses a range of transformation reactions, enabling the efficient synthesis of various biologically active compounds, pharmaceuticals, and agrochemicals.One of the key utilities of $name$ lies in its role as a significant intermediate in the synthesis of heterocyclic compounds, which are essential structural motifs found in many bioactive molecules. Through the utilization of $name$ as a precursor, chemists can access a diverse array of heterocycles such as pyrazoles, pyrimidines, and triazoles, each possessing unique biological activities and pharmacological properties.Furthermore, the reactivity of the aryl ketone moiety in $name$ allows for selective functionalization through various chemical transformations. By harnessing the electrophilic nature of the ketone group, researchers can introduce different substituents onto the phenyl rings, enabling the tailored modification of the molecule for specific synthetic targets or biological studies.In addition, the presence of both an amino and a fluorophenyl group in $name$ offers further opportunities for structural modification and diversity-oriented synthesis. These functionalities can engage in a range of reactions, such as cross-coupling, nucleophilic substitution, and reductive amination, allowing for the creation of complex molecular architectures with precise control over stereochemistry and regioselectivity.Overall, the strategic incorporation of (4-Aminophenyl)(4-fluorophenyl)methanone into chemical synthesis endeavors provides chemists with a powerful tool for accessing structurally diverse compounds with potential applications in drug discovery, material science, and chemical biology.