- BENZYL PHENYL SULFONE
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- $1.00 / 1KG
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2024-08-11
- CAS:3112-88-7
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 20T
- BENZYL PHENYL SULFONE
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- $5.50 / 1KG
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2020-01-13
- CAS:3112-88-7
- Min. Order: 1KG
- Purity: 98%min
- Supply Ability: 1kg-100kg
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| Product Name: | BENZYL PHENYL SULFONE | | Synonyms: | sulfone,benzylphenyl;BENZYL PHENYL SULFONE;BENZYL PHENYL SULPHONE;(Benzylsulfonyl);Benzyl phenyl sulfone, 98+%;Benzy Pheny Sulfone;BENZYL PHENYL SULFON;benzenesulfonylmethylbenzene | | CAS: | 3112-88-7 | | MF: | C13H12O2S | | MW: | 232.3 | | EINECS: | 221-477-3 | | Product Categories: | | | Mol File: | 3112-88-7.mol |  |
| | BENZYL PHENYL SULFONE Chemical Properties |
| Melting point | 146-150 °C | | Boiling point | 344.47°C (rough estimate) | | density | 1.2321 (rough estimate) | | refractive index | 1.5200 (estimate) | | storage temp. | Sealed in dry,Room Temperature | | form | Crystalline Powder | | color | Off-white | | BRN | 2049938 | | CAS DataBase Reference | 3112-88-7(CAS DataBase Reference) |
| | BENZYL PHENYL SULFONE Usage And Synthesis |
| Application | Benzylphenyl sulfone can be used as a pharmaceutical synthesis intermediate. In existing research on the selective oxidation of thioethers to sulfone compounds, acids, metal oxides, organic peroxides, inorganic peroxides, and halogens are commonly used as oxidants. | | Chemical Properties | off-white crystalline powder | | Synthesis Reference(s) | Synthetic Communications, 20, p. 925, 1990 DOI: 10.1080/00397919008052793
Tetrahedron Letters, 8, p. 3299, 1967 | | Synthesis | 100 mLSchlenk reaction tube was sequentially added TEMPO (3.9 mg, 0.025 mmol), methanol (1 mL), CuSO (4.0 mg, 0.025 mmol), 3,5-dimethylpyridine (28.2 L, 0.25 mmol), benzene sulfide (58.8 L, 0.5 mmol), filled with 1 atm oxygen, sealed reaction tube heated to 65 reaction 72h. After the reaction was cooled to room temperature, add appropriate amount of ethyl acetate, the reaction solution of blue solid precipitation, filtration, concentration under reduced pressure, through the column chromatography, the filtrate. The reaction tube was sealed and heated to 65 for 72 h. At the end of the reaction, the reaction was cooled to room temperature, appropriate amount of ethyl acetate was added, and a blue solid was precipitated in the reaction solution, which was filtered, and the filtrate was concentrated under reduced pressure, and purified by column chromatography to obtain the product with a yield of 82%. |
| | BENZYL PHENYL SULFONE Preparation Products And Raw materials |
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