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| | 4-(Trifluoromethyl)thiobenzamide Basic information |
| | 4-(Trifluoromethyl)thiobenzamide Chemical Properties |
| Melting point | 136-137 °C | | Boiling point | 246.0±50.0 °C(Predicted) | | density | 1.372±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,2-8°C | | pka | 12.04±0.29(Predicted) | | form | powder to crystal | | color | Light yellow to Yellow to Green | | Sensitive | Stench | | BRN | 4672885 | | InChI | InChI=1S/C8H6F3NS/c9-8(10,11)6-3-1-5(2-4-6)7(12)13/h1-4H,(H2,12,13) | | InChIKey | IPRFNMJROWWFBH-UHFFFAOYSA-N | | SMILES | C1(C(N)=S)=CC=C(C(F)(F)F)C=C1 | | CAS DataBase Reference | 72505-21-6(CAS DataBase Reference) | | NIST Chemistry Reference | 4-(Trifluoromethyl)thiobenzamide(72505-21-6) |
| Hazard Codes | Xn,Xi,T | | Risk Statements | 20/21/22-36/37/38 | | Safety Statements | 36/37/39-26-22-36 | | RIDADR | 2811 | | Hazard Note | Irritant/Stench | | HazardClass | 6.1 | | PackingGroup | III | | HS Code | 29309090 | | Storage Class | 13 - Non Combustible Solids |
| | 4-(Trifluoromethyl)thiobenzamide Usage And Synthesis |
| Chemical Properties | Yellow crystalline powder | | Synthesis | The general procedure for the synthesis of 4-(trifluoromethyl)thiobenzamide from 4-trifluoromethylbenzonitrile was as follows: 500 mg (2.92 mmol) of 4-trifluoromethylbenzonitrile was reacted with 702 mg (8.7 mmol) of sodium thiohydride for 3 hr at 60 °C. Ethanol was used as a solvent during the reaction, and the ethanol was removed by distillation after the reaction was completed. Subsequently, ethyl acetate was added to the reaction mixture and the resulting solution was washed with water. The organic layer was dried with anhydrous magnesium sulfate and then the solvent was removed by distillation. The residue was purified by column chromatography to give 517 mg (95% yield) of 4-(trifluoromethyl)thiobenzamide. The product could be used in the next step of the reaction without further purification. Mass spectrometry (EI) showed a molecular ion peak of 152 (M++1). | | References | [1] Journal of Medicinal Chemistry, 2014, vol. 57, # 8, p. 3213 - 3222
[2] Patent: WO2005/40127, 2005, A1. Location in patent: Page/Page column 100-101
[3] Journal of Fluorine Chemistry, 2006, vol. 127, # 1, p. 63 - 67
[4] Patent: WO2004/6922, 2004, A1. Location in patent: Page/Page column 27; 28
[5] RSC Advances, 2018, vol. 8, # 1, p. 170 - 175 |
| | 4-(Trifluoromethyl)thiobenzamide Preparation Products And Raw materials |
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