(S)-4-TOLUENESULPHINAMIDE
(S)-4-Methylbezenesulfinamide
CAS: 188447-91-8
Molecular Formula: C7H9NOS
(S)-4-TOLUENESULPHINAMIDE - Names and Identifiers
| Name | (S)-4-Methylbezenesulfinamide |
| Synonyms | (S)-4-TOLUENESULFINAMIDE (S)-4-TOLUENESULPHINAMIDE (S)-4-Methylbezenesulfimide (S)-(+)-P-TOLUENESULFINAMIDE (S)-(+)-p-Toluenesulfinamide (S)-4-Methylbezenesulfinamide (S)-4-METHYL-BENZENESULFINAMIDE (S)-4-Methylbezenesulfinamide (S)-(+)-p-Toluenesulfinamide |
| CAS | 188447-91-8 |
| InChI | InChI=1/C7H9NOS/c1-6-2-4-7(5-3-6)10(8)9/h2-5H,8H2,1H3/t10-/m0/s1 |
(S)-4-TOLUENESULPHINAMIDE - Physico-chemical Properties
| Molecular Formula | C7H9NOS |
| Molar Mass | 155.22 |
| Density | 1.28±0.1 g/cm3(Predicted) |
| Melting Point | 118-121°C(lit.) |
| Boling Point | 0°C |
| Flash Point | 0°C |
| Vapor Presure | 0mmHg at 25°C |
| Appearance | White to light yellow crystal powder |
| pKa | 9.52±0.40(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.65 |
| Physical and Chemical Properties | WGK Germany:3 |
(S)-4-TOLUENESULPHINAMIDE - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S37/39 - Wear suitable gloves and eye/face protection |
| WGK Germany | 3 |
(S)-4-TOLUENESULPHINAMIDE - Introduction
(S)-4-methylbezensulfinamide is a chiral molecule with the chemical formula C8H9NO2S. It is a solid, white crystal at room temperature, soluble in organic solvents such as ethanol and dimethyl sulfoxide.
(S)-4-methylbezensulfinamide has a wide range of applications in biological research. It can be used as a chiral resolution reagent for the preparation of chiral drugs and unnatural amino acids. In addition, it can also be used as a catalyst for the synthesis of chiral catalysts and symmetry breaking reactions.
The method of preparing (S)-4-Methylbezenesulfinamide is usually achieved by aromatic or aliphatic Amination Reactions. For example, P-toluenesulfinyl chloride can be reacted with a chiral amine in the presence of a base to form (S)-4-Methylbezenesulfinamide.
You need to pay attention to its safety when using (S)-4-methylbezensulfinamide. It is a compound that is toxic to the human body, irritating and corrosive. Avoid direct contact with skin, eyes and respiratory tract, and wear appropriate protective equipment. During storage, it should be kept in a dry, cool place and avoid contact with oxidants and acids.
(S)-4-methylbezensulfinamide has a wide range of applications in biological research. It can be used as a chiral resolution reagent for the preparation of chiral drugs and unnatural amino acids. In addition, it can also be used as a catalyst for the synthesis of chiral catalysts and symmetry breaking reactions.
The method of preparing (S)-4-Methylbezenesulfinamide is usually achieved by aromatic or aliphatic Amination Reactions. For example, P-toluenesulfinyl chloride can be reacted with a chiral amine in the presence of a base to form (S)-4-Methylbezenesulfinamide.
You need to pay attention to its safety when using (S)-4-methylbezensulfinamide. It is a compound that is toxic to the human body, irritating and corrosive. Avoid direct contact with skin, eyes and respiratory tract, and wear appropriate protective equipment. During storage, it should be kept in a dry, cool place and avoid contact with oxidants and acids.
Last Update：2024-04-09 20:52:54
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