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AB08550

199103-19-0 | Benzyl 4-((methylsulfonyl)oxy)piperidine-1-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $12.00 $9.00 -   +
5g 98% in stock $16.00 $12.00 -   +
10g 98% in stock $26.00 $19.00 -   +
100g 98% in stock $251.00 $176.00 -   +
500g 98% in stock $875.00 $613.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB08550
Chemical Name: Benzyl 4-((methylsulfonyl)oxy)piperidine-1-carboxylate
CAS Number: 199103-19-0
Molecular Formula: C14H19NO5S
Molecular Weight: 313.3694
MDL Number: MFCD09953312
SMILES: O=C(N1CCC(CC1)OS(=O)(=O)C)OCc1ccccc1

 

Computed Properties
Complexity: 431  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 21  
Hydrogen Bond Acceptor Count: 5  
Rotatable Bond Count: 5  
XLogP3: 1.6  

 

 

Upstream Synthesis Route
  • Benzyl 4-((methylsulfonyl)oxy)piperidine-1-carboxylate is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. Its primary application lies in the realm of organic chemistry, where it serves as a vital building block in the creation of various complex molecules. The presence of the benzyl group and the piperidine ring in the structure of this compound confers significant advantages in synthetic processes.In chemical synthesis, Benzyl 4-((methylsulfonyl)oxy)piperidine-1-carboxylate functions as a key intermediate for the construction of a diverse range of organic compounds. Its reactivity allows for efficient and selective manipulation, making it an essential component in the creation of pharmaceuticals, agrochemicals, and other fine chemicals. By utilizing this compound as a starting material or intermediate, chemists can access a multitude of pathways to synthesize intricate molecules with tailored properties and functionalities.Furthermore, the presence of the methylsulfonyl group in Benzyl 4-((methylsulfonyl)oxy)piperidine-1-carboxylate enhances its utility in chemical transformations, enabling a wide array of synthetic strategies such as nucleophilic substitutions, palladium-catalyzed coupling reactions, and radical reactions. The versatile nature of this compound makes it a valuable tool for medicinal chemists, process chemists, and researchers seeking to explore new synthetic pathways and develop novel compounds with diverse applications.
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