CF0023
4-Bromophenoxytetrafluoethyl trimethylsilane
form
liquid
reaction suitability
reaction type: C-C Bond Formation
Application
After being activated with silicophilic activators, like fluorides, alkoxides or carboxylates, 4-bromophenoxytetrafluoroethyl trimethylsilane serves as a nucleophilic source of the 4-bromophenoxytetrafluoroethyl moiety in reaction with electrophiles such as aromatic aldehydes. The aromatic bromide can be used to build up molecular complexity using Pd-catalyzed cross couplings.
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Legal Information
Product of CF Plus Chemicals.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
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Articles
Fluoroalkylation toolbox expands with various reagents for late-stage fluoroalkylation in organic synthesis and medicinal chemistry.
目前的氟烷基化工具包括Togni试剂、高价碘全氟烷基化试剂、氟烷基溴化物、硅烷类和羧酸盐类以及用于后期氟烷基化的磺酰氟类。
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