196929-78-9
Chemical Structure
(R)-(+)-tert-Butylsulfinamide
Synonym(s): (R)-2-Methylpropane-2-sulfinamide
- CAS No.: 196929-78-9
- Formula:C4H11NOS
- Molecular Weight:121.20
IUPAC Name: (R)-2-methylpropane-2-sulfinamide
InChIKey: CESUXLKAADQNTB-SSDOTTSWSA-N
SMILES: CC([S@](N)=O)(C)C
Biological Activity: (R)-(+)-tert-Butylsulfinamide ((R)-2-Methylpropane-2-sulfinamide) is a chiral reagent commonly used in the asymmetric synthesis of compounds such as amines, amino acids, and amino alcohols. (R)-(+)-tert-Butylsulfinamide achieves stereoselective reactions by condensing with carbonyl groups to form sulfinyl imine intermediates, and after the reaction, this group can be removed under acidic conditions to obtain the target product[1][2].
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(R)-(+)-tert-Butylsulfinamide | 99.95% | (R)-(+)-tert-Butylsulfinamide ((R)-2-Methylpropane-2-sulfinamide) is a chiral reagent commonly used in the asymmetric synthesis of compounds such as amines, amino acids, and amino alcohols. (R)-(+)-tert-Butylsulfinamide achieves stereoselective reactions by condensing with carbonyl groups to form sulfinyl imine intermediates, and after the reaction, this group can be removed under acidic conditions to obtain the target product. | ||||||||||||||||||||
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Keywords
