124401-11-2

Basic information

• Product Name: 7b-phenyl-7bH-oxazirino<2,3-b><1,2>benzisothiazole 3,3-dioxide
• Synonyms: 7b-phenyl-7bH-oxazirino<2,3-b><1,2>benzisothiazole 3,3-dioxide
• CAS NO: 124401-11-2
• Molecular Weight: 259.285
• Mol File: 124401-11-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 7b-phenyl-7bH-oxazirino<2,3-b><1,2>benzisothiazole 3,3-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 7b-phenyl-7bH-oxazirino<2,3-b><1,2>benzisothiazole 3,3-dioxide(124401-11-2)
• EPA Substance Registry System: 7b-phenyl-7bH-oxazirino<2,3-b><1,2>benzisothiazole 3,3-dioxide(124401-11-2)

Safety Data

• Hazardous Substances Data: 124401-11-2(Hazardous Substances Data)

Upstream product

• 53440-57-6 3-phenylbenzo[d]isothiazole-1,1-dioxide 
• 591-51-5 phenyllithium 
• 81-07-2 saccharin 
• 1345021-05-7 3-(4-bromophenyl)-1,2-benzoisothiazole 1,1-dioxide 
• 100-58-3 phenylmagnesium bromide 
• 567-19-1 3-chloro-1,2-benzisothiazole 1,1-dioxide 
• 18712-15-7 3-ethoxy-benzo[d]isothiazole 1,1-dioxide 

Downstream Products

• 296776-36-8 (S)-3-phenyl-2,3-dihydrobenzo[d]isothiazole 1,1-dioxide 
• 296776-37-9 (R)-3-phenyl-2,3-dihydrobenzo[d]isothiazole 1,1-dioxide 
• 53440-57-6 3-phenylbenzo[d]isothiazole-1,1-dioxide 
• 3112-85-4 methylphenylsulfonate 

Relevant articles and documents

Enantioselective organocatalytic oxidation of ketimine

C3-Symmetric chiral trisimidazolines with m-chloroperbenzoic acid promoted the organocatalytic oxidation of N-sulfonyl ketimine. The present imidazoline catalysis produced oxaziridines bearing a tetrasubstituted carbon stereogenic center in hig

Iron(iii)-salan complexes catalysed highly enantioselective fluorination and hydroxylation of β-keto esters and N-Boc oxindoles

Chiral iron(iii)-salan complexes catalysed highly enantioselective α-fluorination and α-hydroxylation of β-keto esters and N-Boc oxindoles to give the corresponding products in high yields and good-to-excellent ee values under mild reaction conditions. This journal is the Partner Organisations 2014.

Selective 1,4-Chiral Induction in the Reaction of Enolates Generated from t-Butyl δ-Hydroxy Carboxylates

Lithium enolates generated from t-butyl esters of δ-hydroxy carboxylic acids with lithium dialkylamides in THF-HMPA were alkylated stereoselectively to give the corresponding syn-α-alkylated δ-hydroxy esters.The generation of the enolates was accelerated by the addition of lithium trifluoromethanesulfonate, and the successive aldol and hydroxylation reactions of the enolates also proceeded in a stereoselective manner.