120484-50-6 | 1-(2-Fluoro-6-methoxyphenyl)ethanone

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$10.00	$7.00
5g	97%	in stock	$14.00	$10.00

Description

• Catalog Number: AB62196
• Chemical Name: 1-(2-Fluoro-6-methoxyphenyl)ethanone
• CAS Number: 120484-50-6
• Molecular Formula: C9H9FO2
• Molecular Weight: 168.165
• MDL Number: MFCD00671762
• SMILES: COc1cccc(c1C(=O)C)F

Computed Properties

• Complexity: 170
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• XLogP3: 1.7

Upstream Synthesis Route

1-(2-Fluoro-6-methoxyphenyl)ethanone is a versatile organic compound that finds wide application in chemical synthesis. This compound is commonly utilized as a building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure, characterized by the presence of both a fluorine atom and a methoxy group on the phenyl ring, imparts specific reactivity and selectivity in synthetic transformations.In chemical synthesis, 1-(2-Fluoro-6-methoxyphenyl)ethanone serves as a key intermediate in the preparation of diverse heterocyclic compounds, which are essential structural motifs in many biologically active molecules. The presence of the fluoro and methoxy substituents enables the introduction of functional groups at specific positions, allowing for precise molecular modifications. These modifications can lead to the development of new drug candidates, pesticides, and other valuable compounds with enhanced properties.Moreover, the reactivity of 1-(2-Fluoro-6-methoxyphenyl)ethanone in various coupling reactions, such as Suzuki, Heck, and Buchwald-Hartwig cross-coupling reactions, makes it a valuable tool for constructing complex molecular architectures. By participating in these transformations, this compound can facilitate the formation of carbon-carbon and carbon-heteroatom bonds, enabling the efficient synthesis of structurally diverse organic compounds.Overall, the application of 1-(2-Fluoro-6-methoxyphenyl)ethanone in chemical synthesis showcases its utility as a versatile building block for the preparation of valuable molecules with potential applications in the pharmaceutical, agrochemical, and materials science industries.