| CAS: | 83015-33-2 | |
| 分子式: | C8H5BrF4S | |
| 分子量: | 289.09 | |
| 英文名称: |
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| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||
| B975024 | MACKLIN | (2-溴-1,1,2,2-四氟-乙基)硫基苯 | 95% | 427元/100mg; 709元/250mg; 2286元/1g; | 展开 | ||||||||||||||||||||||||
储存:2-8°C, 干燥 | |||||||||||||||||||||||||||||
| CF0014 | Sigma-Aldrich | Phenylsulfanyltetrafluorobromoethane | 5697.82元/1 G; | 展开 | |||||||||||||||||||||||||
产品说明 应用 Phenylsulfanyltetrafluoroethyl bromide is a fluoroalkylbromide that is a radical source of the phenylsulfanyltetrafluoroethyl moiety. Alternatively, it can also be selectively metallated at the fluorinated carbon with Turbo Grignard reagent at low temperatures resulting in a thermally unstable anion that can act as a nucleophilic fluoroalkylation reagent towards a wide variety of electrophiles, such as aldehydes, ketones or sulfonylimines. A phenylsulfanyltetrafluoroethyl moiety incorporated in the substrate can be treated with tributyltin hydride and generate the corresponding fluoroalkyl radical. If the substrate lacks any olefins, it can be reduced to tetrafluoroethyl group whereas if the substrate contains an olefin in a correct spatial orientation, it can lead to an intramolecular cyclization affording tetrafluorinated cyclic structures. 其他说明 Technology Spotlight: Fluoroalkylation: Expansion of Togni Reagents 法律信息 Product of CF Plus Chemicals. 基本信息
产品性质
安全信息
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