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AA09087

1023-17-2 | 4'-Methoxy-2-phenylacetophenone

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $7.00 $5.00 -   +
1g 98% in stock $13.00 $9.00 -   +
5g 98% in stock $15.00 $11.00 -   +
10g 98% in stock $29.00 $21.00 -   +
25g 98% in stock $72.00 $51.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA09087
Chemical Name: 4'-Methoxy-2-phenylacetophenone
CAS Number: 1023-17-2
Molecular Formula: C15H14O2
Molecular Weight: 226.2705
MDL Number: MFCD00017177
SMILES: COc1ccc(cc1)C(=O)Cc1ccccc1
NSC Number: 26658

 

Computed Properties
Complexity: 235  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 2  
Rotatable Bond Count: 4  
XLogP3: 3.2  

 

 

Upstream Synthesis Route
  • 1-(4-Methoxyphenyl)-2-phenylethanone, also known as acetophenone derivative, plays a crucial role in chemical synthesis as a versatile building block. This compound is widely utilized in organic chemistry for its unique reactivity and functional group compatibility. Specifically, 1-(4-Methoxyphenyl)-2-phenylethanone is commonly employed as a precursor in the synthesis of various complex organic molecules.In chemical synthesis, this compound serves as a key intermediate in the preparation of biologically active compounds, pharmaceuticals, agrochemicals, and fragrances. Its structural flexibility allows for the introduction of different substituents and modifications, enabling the creation of diverse chemical structures with specific properties and functions. Additionally, the presence of both aromatic rings in 1-(4-Methoxyphenyl)-2-phenylethanone offers opportunities for further derivatization through various functional group manipulations.Furthermore, the reactivity of 1-(4-Methoxyphenyl)-2-phenylethanone enables chemists to conduct a range of transformations, such as reduction, oxidation, and functional group interconversions. This compound's ability to participate in carbon-carbon bond formation reactions, including Friedel-Crafts acylation and aldol condensations, enhances its utility in the synthesis of complex organic molecules.Overall, 1-(4-Methoxyphenyl)-2-phenylethanone is a valuable building block in chemical synthesis due to its reactivity, versatility, and ability to facilitate the construction of diverse organic frameworks with tailored properties and functionalities.
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