1-(Phenylsulfanyl)-4-(trifluoromethyl)benzene
4-Trifluoromethyldiphenyl sulfide
CAS: 53451-90-4
Molecular Formula: C13H9F3S
1-(Phenylsulfanyl)-4-(trifluoromethyl)benzene - Names and Identifiers
1-(Phenylsulfanyl)-4-(trifluoromethyl)benzene - Physico-chemical Properties
| Molecular Formula | C13H9F3S |
| Molar Mass | 254.27 |
| Density | 1.29±0.1 g/cm3(Predicted) |
| Melting Point | 36 °C |
| Boling Point | 314.8±42.0 °C(Predicted) |
| Flash Point | 144.2°C |
| Vapor Presure | 0.000841mmHg at 25°C |
| Refractive Index | 1.57 |
| Physical and Chemical Properties | Light yellow crystals. |
1-(Phenylsulfanyl)-4-(trifluoromethyl)benzene - Introduction
4-Trifluoromethyldiphenyl sulfide is an organic compound with the chemical formula C13H9F3S. It is colorless to pale yellow crystals, soluble in common organic solvents such as ethanol, dimethylformamide and dichloromethane.
4-Trifluoromethyldiphenyl sulfide is commonly used as a reagent in organic synthesis. It can participate in electrophilic substitution or nucleophilic reactions, such as substitution reactions with halogenated hydrocarbons, resulting in new compounds. In addition, it can also be used in the synthesis of heterocyclic compounds or pesticides and other active molecules.
There are various methods for preparing 4-Trifluoromethyldiphenyl sulfide, one of which is commonly used by the reaction of diphenyl sulfide and trifluoromethyl mercaptan. The reaction is generally carried out under an inert atmosphere or at a low temperature to improve the yield.
Regarding safety information, 4-Trifluoromethyldiphenyl sulfide has low toxicity, but it is still necessary to pay attention to safe operation. During use or storage, contact with strong oxidants should be avoided to avoid harmful substances. At the same time, care should be taken to avoid inhaling its vapor or dust, and avoid contact with skin and eyes. Wear appropriate personal protective equipment such as goggles and gloves during handling. For accidental poisoning or exposure, seek medical attention immediately and bring a container or label. In addition, the 4-Trifluoromethyldiphenyl sulfide should be stored in a cool, dry place, away from ignition and flammable materials.
4-Trifluoromethyldiphenyl sulfide is commonly used as a reagent in organic synthesis. It can participate in electrophilic substitution or nucleophilic reactions, such as substitution reactions with halogenated hydrocarbons, resulting in new compounds. In addition, it can also be used in the synthesis of heterocyclic compounds or pesticides and other active molecules.
There are various methods for preparing 4-Trifluoromethyldiphenyl sulfide, one of which is commonly used by the reaction of diphenyl sulfide and trifluoromethyl mercaptan. The reaction is generally carried out under an inert atmosphere or at a low temperature to improve the yield.
Regarding safety information, 4-Trifluoromethyldiphenyl sulfide has low toxicity, but it is still necessary to pay attention to safe operation. During use or storage, contact with strong oxidants should be avoided to avoid harmful substances. At the same time, care should be taken to avoid inhaling its vapor or dust, and avoid contact with skin and eyes. Wear appropriate personal protective equipment such as goggles and gloves during handling. For accidental poisoning or exposure, seek medical attention immediately and bring a container or label. In addition, the 4-Trifluoromethyldiphenyl sulfide should be stored in a cool, dry place, away from ignition and flammable materials.
Last Update：2024-04-10 22:29:15
