Molecular Formula | C4H11NOS |
Molar Mass | 121.2 |
Density | 0.903 g/mL at 25 °C |
Melting Point | 103-107°C(lit.) |
Boling Point | 220.0±23.0 °C(Predicted) |
Specific Rotation(α) | 4 º (c=1, CHCl3 + amylenes) |
Flash Point | -17℃ |
Solubility | Soluble in chloroform, methanol, tetrahydrofuran, dichloromethane, dimethyl sulfoxide and most organic solvents. |
Appearance | Crystallization |
Color | White, light pink, light yellow to brown |
pKa | 10.11±0.50(Predicted) |
Storage Condition | 2-8°C |
Stability | store cold |
Refractive Index | 4 ° (C=1, CHCl3) |
MDL | MFCD05861479 |
Use | Used as an intermediate in organic synthesis |
Risk Codes | R11 - Highly Flammable R19 - May form explosive peroxides R36/37 - Irritating to eyes and respiratory system. R40 - Limited evidence of a carcinogenic effect R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. S36/37 - Wear suitable protective clothing and gloves. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S16 - Keep away from sources of ignition. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
UN IDs | UN 2056 3 / PGII |
WGK Germany | 3 |
TSCA | No |
HS Code | 29309090 |
Hazard Note | Irritant/Keep Cold |
Use | (R)-( )-tert-butyl sulfinamide is a chiral ligand used in pharmaceutical compositions. (R)-(+)-tert-butyl sulfinamide can be easily converted to P,N-sulfinyl imine ligands by condensation with aldehydes and ketones that can undergo iridium-catalyzed asymmetric hydrogenation of olefins. Used as an intermediate in organic synthesis A reagent for the synthesis of chiral amines. |