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AA12414

1138-56-3 | 4-(N-Butoxy)benzenesulfonyl chloride

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $13.00 $9.00 -   +
1g 98% in stock $21.00 $15.00 -   +
5g 98% in stock $53.00 $37.00 -   +
25g 98% in stock $260.00 $182.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA12414
Chemical Name: 4-(N-Butoxy)benzenesulfonyl chloride
CAS Number: 1138-56-3
Molecular Formula: C10H13ClO3S
Molecular Weight: 248.7264
MDL Number: MFCD00052344
SMILES: CCCCOc1ccc(cc1)S(=O)(=O)Cl

 

Computed Properties
Complexity: 263  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 5  
XLogP3: 3.5  

 

 

Upstream Synthesis Route
  • 4-Butoxybenzene-1-sulfonyl chloride, also known as butyl 4-sulfonylbenzoate, is a versatile intermediate in chemical synthesis widely used in pharmaceutical and agrochemical industries. This compound serves as a key building block for the introduction of the sulfonyl group (-SO2Cl) into organic molecules, allowing for the creation of diverse chemical structures with valuable properties.In chemical synthesis, 4-Butoxybenzene-1-sulfonyl chloride is commonly employed as a sulfonylating reagent for the functionalization of various substrates. It can react with nucleophiles such as amines, alcohols, and thiols, leading to the formation of sulfonylated products. This sulfonyl chloride is particularly useful in the preparation of sulfonamides, a class of compounds with important biological activities, including antimicrobial and anticancer properties.Furthermore, 4-Butoxybenzene-1-sulfonyl chloride can be utilized in the construction of complex organic molecules through sulfonyl group transfer reactions. By selectively modifying specific functional groups within a molecule, this compound enables chemists to tailor the properties of the final products for target applications. Its compatibility with a variety of reaction conditions and its ability to introduce the sulfonyl functionality make it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.
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