(R)-tert-Butylsulfinamide

CAS : 196929-78-9

Ref. TR-B693760

Informations sur le produit

• Nom: (R)-tert-Butylsulfinamide
• Synonymes: (R)-(+)-2-Methyl-2-propanesulfinamide, (R)-N-tert-Butanesulfinamide, (R)-(+)-2-Methyl-2-Propanesulfinamide, (R)-(+)-2-Methyl-Propane-2-Sulfinic Acid Amide, (R)-(+)-2-Methylpropane-2-Sulphinamide, (R)-(+)-Methyl-2-Propanesulfinamide, (R)-(+)-T-Butanesulfinamide, (R)-(+)-T-Butyl Sulfinamide, (R)-(+)-T-Butylmethylsulfinamide, (R)-(+)-T-Butylsulfinamide, (R)-(+)-Tert-Butanesulfinamide, (R)-(+)-Tert-Butyl Sulphinamide, (R)-2-Methylpropan-2-sulfinamide, (R)-2-Methylpropane-2-Sulfinamide, (R)-N-Tert-Butanesulfinamide, 2-Propanesulfinamide, 2-methyl-, (R)-, 2-Propanesulfinamide, 2-methyl-, [S(R)]-, R-(+)-Tert-Butansulfinamide, [S(R)]-2-Methyl-2-propanesulfinamide
• CAS: 196929-78-9

Description

Applications (R)-tert-Butylsulfinamide is a chiral ligand used in pharmaceutical compositions. (R)-tert-Butylsulfinamide can be readily transformed into P,N-sulfinyl imine ligands through condensation with aldehydes and ketones, which can undergo iridium-catalyzed asymmetric hydrogenation of olefins.
References Szallasi, A., et al.: Pharmacol. Rev., 51, 159 (1999), Montell, C., et al.: Mol. Cell., 9, 229 (2002), Ryu, C., et al.: Bioorg. Med. Chem. Lett., 14, 1751 (2004), Suh, Y., et al.: J. Med. Chem., 48, 5823 (2005),

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 121.20
• Formule: C₄H₁₁NOS
• Couleur/Forme: White to Yellow Solid
• InChI: InChI=1S/C4H11NOS/c1-4(2,3)7(5)6/h5H2,1-3H3/t7-/m1/s1
• Code InChI: InChIKey=CESUXLKAADQNTB-SSDOTTSWSA-N
• SMILES: CC(C)(C)[S@](N)=O