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AB66022

10297-73-1 | 4-Methylsulphonylacetophenone

Packsize Purity Availability Price Discounted Price    Quantity
5g 97% in stock $6.00 $4.00 -   +
10g 97% in stock $7.00 $5.00 -   +
25g 97% in stock $13.00 $9.00 -   +
100g 97% in stock $32.00 $22.00 -   +
500g 97% in stock $156.00 $109.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB66022
Chemical Name: 4-Methylsulphonylacetophenone
CAS Number: 10297-73-1
Molecular Formula: C9H10O3S
Molecular Weight: 198.2389
MDL Number: MFCD00025072
SMILES: CC(=O)c1ccc(cc1)S(=O)(=O)C
NSC Number: 403928

 

Computed Properties
Complexity: 279  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 2  
XLogP3: 0.9  

 

 

Upstream Synthesis Route
  • 4'-(Methylsulfonyl)acetophenone is a versatile organic compound that finds significant application in chemical synthesis. Its unique structure makes it a valuable building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals.One of the key uses of 4'-(Methylsulfonyl)acetophenone is as a starting material for the synthesis of different sulfur-containing compounds. By utilizing the methylsulfonyl group, chemists can introduce sulfur atoms into the molecular structure, leading to the formation of compounds with diverse properties and functionalities. This compound serves as a key intermediate in the preparation of sulfonamide derivatives, which are important in medicinal chemistry.Additionally, 4'-(Methylsulfonyl)acetophenone is employed in the synthesis of chiral ligands and catalysts. Its presence in the molecular structure can impart specific stereochemical properties, making it useful in asymmetric synthesis and catalysis. This compound plays a crucial role in the development of new methodologies for organic transformations and the production of enantiomerically pure compounds.Furthermore, 4'-(Methylsulfonyl)acetophenone can be utilized as a masking group for carbonyl compounds in organic synthesis. The methylsulfonyl moiety can protect a carbonyl functionality from unwanted reactions, allowing selective modifications in multi-step synthetic sequences. This property makes it a valuable tool in the construction of complex organic molecules and natural product synthesis.Overall, the versatility and reactivity of 4'-(Methylsulfonyl)acetophenone make it a valuable reagent in chemical synthesis, enabling the preparation of diverse functionalized compounds with applications across various fields of chemistry.
Literature
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