trans-1,2-Bis(phenylsulfonyl)ethylene

CAS: 963-16-6

Ref. 3D-FB61268

Produktinformation

• Name: trans-1,2-Bis(phenylsulfonyl)ethylene
• Synonyme: (E)-1,2-Bis(benzenesulfonyl)ethylene, (E)-1,2-Bis(phenylsulfonyl)ethene, (E)-1,2-Bis(phenylsulfonyl)ethylene, (E)-1,2-Di(phenylsulfonyl)ethene, (E)-1,2-Di(phenylsulfonyl)ethylene, ([(E)-2-(Phenylsulfonyl)ethenyl]sulfonyl)benzene, 1,1'-[(E)-ethene-1,2-diyldisulfonyl]dibenzene, 1,1′-[(1E)-1,2-Ethenediylbis(sulfonyl)]bis[benzene], Benzene, 1,1′-[(1E)-1,2-ethenediylbis(sulfonyl)]bis-, Benzene, 1,1′-[1,2-ethenediylbis(sulfonyl)]bis-, (E)-, Ethene, 1,2-bis(phenylsulfonyl)-, Ethylene, 1,2-bis(phenylsulfonyl)-, (E)-, NSC 202471, benzene, 1,1'-[(E)-1,2-ethenediyldisulfonyl]bis-, trans-1,2-Bis(benzenesulfonyl)ethene, trans-1,2-Bis(phenylsulfonyl)ethene, trans-1,2-Di(phenylsulfonyl)ethylene, trans-Bis(phenylsulfonyl)ethylene

Beschreibung

Trans-1,2-Bis(phenylsulfonyl)ethylene is a chiral sulfoxide that is used for the synthesis of sulfoxides. It has been shown to be an organocatalyst for reductive elimination and alkenylation reactions. Trans-1,2-Bis(phenylsulfonyl)ethylene is stable under acidic conditions and catalyzes the reaction of persulfate with various compounds to produce sulfates. It can also be used as a chiral synthon in organic synthesis. Trans-1,2-Bis(phenylsulfonyl)ethylene reacts with an aldehyde or ketone in the presence of base to form a sulfoxide. This reaction proceeds by a nucleophilic addition followed by reductive elimination. The x-ray structures and molecular modelling data obtained from this compound are consistent with the proposed mechanism.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 308.37 g/mol
• Formel: C₁₄H₁₂O₄S₂
• Reinheit: Min. 95%
• InChl: InChI=1S/C14H12O4S2/c15-19(16,13-7-3-1-4-8-13)11-12-20(17,18)14-9-5-2-6-10-14/h1-12H/b12-11+
• InChI Key: InChIKey=YGBXMKGCEHIWMO-VAWYXSNFSA-N
• SMILES: O=S(=O)(/C=C/S(=O)(=O)c1ccccc1)c1ccccc1