p-Toluenesulfonamide

p-Toluenesulfonamide undergoes FeCl3-catalyzed direct substitution reaction with benzylic and allylic alcohols. It is employed as nucleophile in tetrabutylammonium fluoride (TBAF) catalyzed vinyl aziridine opening reaction.

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Catalog Number CBB1112019
Molecular Formula CH3C6H4SO2NH2
CAS# 70-55-3
Purity >98%
Inchi 1S/C7H9NO2S/c1-6-2-4-7(5-3-6)11(8,9)10/h2-5H,1H3,(H2,8,9,10)
Inchi Key LMYRWZFENFIFIT-UHFFFAOYSA-N
SMILES Cc1ccc(cc1)S(N)(=O)=O
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p-Toluenesulfonamide

Cyanomethylenetributylphosphorane (CMBP)-mediated reaction of p-toluenesulfonamide with alcohols has been investigated.

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Catalog Number CBB1112020
Molecular Formula CH3C6H4SO2NH2
CAS# 70-55-3
Purity >99%
Inchi 1S/C7H9NO2S/c1-6-2-4-7(5-3-6)11(8,9)10/h2-5H,1H3,(H2,8,9,10)
Inchi Key LMYRWZFENFIFIT-UHFFFAOYSA-N
SMILES Cc1ccc(cc1)S(N)(=O)=O
Size Inquiry
Supplier Page https://www.amerigoscientific.com/p-toluenesulfonamide-item-112020.html