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AA56089

122539-74-6 | Ethyl 2-(trifluoromethylsulfonyloxy)cyclopent-1-enecarboxylate

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $140.00 $98.00 -   +
1g 95% in stock $211.00 $148.00 -   +
5g 95% in stock $744.00 $521.00 -   +
10g 95% in stock $1,249.00 $874.00 -   +
25g 95% in stock $2,345.00 $1,642.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA56089
Chemical Name: Ethyl 2-(trifluoromethylsulfonyloxy)cyclopent-1-enecarboxylate
CAS Number: 122539-74-6
Molecular Formula: C9H11F3O5S
Molecular Weight: 288.2408
MDL Number: MFCD00209586
SMILES: CCOC(=O)C1=C(CCC1)OS(=O)(=O)C(F)(F)F

 

Computed Properties
Complexity: 458  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 8  
Rotatable Bond Count: 5  
XLogP3: 2.1  

 

 

Upstream Synthesis Route
  • Ethyl 2-(((trifluoromethyl)sulfonyl)oxy)cyclopent-1-enecarboxylate is a versatile compound widely used in chemical synthesis for the preparation of pharmaceuticals, agrochemicals, and various fine chemicals. Its unique structure and functional groups make it a valuable building block in organic chemistry.One key application of Ethyl 2-(((trifluoromethyl)sulfonyl)oxy)cyclopent-1-enecarboxylate is as a reagent in the synthesis of complex organic molecules. Its trifluoromethylsulfonyl moiety can serve as a masked sulfonyl group that can be selectively cleaved under specific conditions to reveal a free sulfonyl group, enabling further functionalization of the molecule. This reactivity profile makes it particularly useful in designing efficient synthetic routes for target compounds.Additionally, the cyclopentene framework of Ethyl 2-(((trifluoromethyl)sulfonyl)oxy)cyclopent-1-enecarboxylate can participate in various cycloaddition reactions, ring-opening reactions, and cross-coupling reactions, allowing for the construction of diverse molecular architectures with high regio- and stereoselectivity.Overall, Ethyl 2-(((trifluoromethyl)sulfonyl)oxy)cyclopent-1-enecarboxylate is a valuable tool in the arsenal of synthetic chemists, enabling the efficient and controlled introduction of functional groups and structural motifs into complex molecules for various applications in the pharmaceutical, agricultural, and chemical industries.
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