AA09087
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 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
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 |
Complexity: | 235 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 17 |
Hydrogen Bond Acceptor Count: | 2 |
Rotatable Bond Count: | 4 |
XLogP3: | 3.2 |
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.