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Home  > Chemistry  > Organic Building Blocks  > Ketones  > 4-(4-Methoxyphenyl)-2-butanone

AB65840

104-20-1 | 4-(4-Methoxyphenyl)-2-butanone

Packsize Purity Availability Price Discounted Price    Quantity
10g 95% in stock $16.00 $12.00 -   +
25g 95% in stock $20.00 $14.00 -   +
100g 95% in stock $61.00 $43.00 -   +
250g 95% in stock $151.00 $106.00 -   +
500g 95% in stock $190.00 $133.00 -   +
1kg 95% in stock $335.00 $235.00 -   +
5kg 95% in stock $825.00 $577.00 -   +
10kg 95% in stock $1,310.00 $917.00 -   +
25kg 95% in stock $2,867.00 $2,007.00 -   +
50kg 95% in stock $5,413.00 $3,789.00 -   +
200kg 95% in stock $14,461.00 $10,123.00 -   +

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*All prices are in USD.

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Description
Catalog Number: AB65840
Chemical Name: 4-(4-Methoxyphenyl)-2-butanone
CAS Number: 104-20-1
Molecular Formula: C11H14O2
Molecular Weight: 178.2277
MDL Number: MFCD00008791
SMILES: COc1ccc(cc1)CCC(=O)C
NSC Number: 405366

 

Computed Properties
Complexity: 158  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 2  
Rotatable Bond Count: 4  
XLogP3: 2.1  

 

 

Upstream Synthesis Route 
  • The organic compound 4-(4-Methoxyphenyl)-2-butanone, also known as p-anisyl methyl ketone, plays a crucial role in chemical synthesis as a versatile building block. It is commonly used as a key intermediate in the preparation of various pharmaceuticals, fragrances, and other fine chemicals. This compound is valued for its ability to serve as a precursor in the synthesis of complex molecules due to its unique structural features. The presence of both an aryl group and a carbonyl functional group in its chemical structure allows for a wide range of chemical transformations, making it a valuable starting material in organic synthesis. In chemical reactions, 4-(4-Methoxyphenyl)-2-butanone can undergo processes such as nucleophilic addition, acylation, and condensation reactions to yield a variety of products. Its reactivity and selectivity in these reactions make it an indispensable tool for chemists seeking to construct intricate molecular structures.Furthermore, the aromatic nature of the 4-methoxyphenyl group provides opportunities for diversification through aromatic substitution reactions, enabling the introduction of additional functional groups or stereochemical complexity to the final compounds. This makes 4-(4-Methoxyphenyl)-2-butanone a valuable building block for creating a wide range of molecules with tailored properties.Overall, the application of 4-(4-Methoxyphenyl)-2-butanone in chemical synthesis offers chemists a versatile and powerful tool for the design and production of various organic compounds with desired functionalities and properties.
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