Name | 3-Chlorophenylmethanesulfonyl chloride |
Synonyms | 3-Chlorophenylmethanesulfonyl chloride 3-Chloro-alpha-toluenesulfonyl chloride (3-chlorophenyl)methanesulfonyl chloride (3-CHLORO-PHENYL)-METHANESULFONYL CHLORIDE (3-Chloro-Phenyl)-Methanesulfonyl Chloride BENZENEMETHANESULFONYL CHLORIDE, 3-CHLORO- |
CAS | 24974-73-0 |
InChI | InChI=1/C7H6Cl2O2S/c8-7-3-1-2-6(4-7)5-12(9,10)11/h1-4H,5H2 |
Molecular Formula | C7H6Cl2O2S |
Molar Mass | 225.09 |
Density | 1.499±0.06 g/cm3(Predicted) |
Melting Point | 69-72°C |
Boling Point | 321.2±25.0 °C(Predicted) |
Flash Point | 148°C |
Vapor Presure | 0.000569mmHg at 25°C |
Storage Condition | Room Temprature |
Sensitive | Moisture Sensitive |
Refractive Index | 1.578 |
MDL | MFCD02683111 |
Risk Codes | R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. R34 - Causes burns R22 - Harmful if swallowed |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
UN IDs | 3261 |
Hazard Class | 8 |
Packing Group | II |
Application | (3-chlorophenyl) methyl sulfonyl chloride is a sulfonyl chloride compound. Sulfonyl chloride compounds are a kind of very important compounds, which are widely used as intermediates and raw materials for organic and drug synthesis, and are important sources of sulfonyl groups. |
preparation | (3-chlorophenyl) methyl sulfonyl chloride is prepared as follows: thiourea (0.387g,5mmol) and m-chlorobenzyl chloride (5mmol) are dissolved in 5mL of ethanol, and after refluxing for 30min, the solvent is removed under reduced pressure to obtain a white solid. This white solid was slowly added dropwise to a mixed system of NaClO2(1.61g,15mmol,85% purity), concentrated HCl(3mL) and MeCN(10mL). During the feeding process, the temperature in the reaction system was controlled by water bath between 10 and 20oC. After the feeding is completed, the stirring reaction is continued for 30min, acetonitrile is removed under reduced pressure under low temperature conditions, 25mL of water is added, the solid in the system is filtered, and the colorless crystal (3-chlorophenyl) methylsulfonyl chloride is obtained by drying, the melting point is 76~78 ℃,1.035g, and the yield is 92%. |