(S)-(-)-t-Butylsulfinamide |
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| Synonyms: (S)-(-)-2-Methyl-propane-2-sulfinic acid amide | |
| Cat. No.: CR00002 | CAS No.: 343338-28-3 |
| MDL.: MFCD05861480 | Formula: (CH3)3CS(O)NH2 |
| F.W.121.20 | Purity: |
| Storage: | |
| Size/Unit | Price | Qty | Availability | Price Total |
|---|---|---|---|---|
| 1g | $65.00 | Enter qty and click checkbox |
 
|
$65.00 |
| 5g | $205.00 | Enter qty and click checkbox |
|
$205.00 |
| Catalog Number： | CR00002 | CAS No.: | 343338-28-3 | |
| MDL: | MFCD05861480 | Formula: | (CH3)3CS(O)NH2 | |
| F.W.: | 121.20 | Purity: | ||
| Package: | Unit: | g | ||
| Appearance: | M.P.: | 97-101 °C(lit.) | ||
| B.P.: | Density: | |||
| Optical Rotation: | [a]20/D -4.5°, c = 1 in chloroform | Refractive Index: | ||
| Solubility: | Stability: | |||
| Storage: | Category: | Chiral Reagents | ||
| Reference: | 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.1 Chiral auxiliary used in an asymmetric preparation of trifluoroethylamines by conversion of trifluoroacetaldehyde to a chiral imine followed by treatment with an aryl lithium and acidic methanolysis. Useful reagent for synthesizing chiral amines. | |||