form
liquid
reaction suitability
reaction type: C-C Bond Formation
SMILES string
FC(F)(Br)C(F)(F)Oc1ccc(cc1)Br
InChI
1S/C8H4Br2F4O/c9-5-1-3-6(4-2-5)15-8(13,14)7(10,11)12/h1-4H
InChI key
MHPXJSIMKFXETB-UHFFFAOYSA-N
Application
4-Bromophenoxytetrafluoroethyl bromide is a fluoroalkylbromide that is a radical source of the 4-bromophenoxytetrafluoroethyl 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.The aromatic bromide can be further subjected to Pd-catalyzed cross-coupling reactions to build molecular complexity.
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Legal Information
Product of CF Plus Chemicals.
存储类别
10 - Combustible liquids
怎么回事？
WGK 3
闪点 (F)
Not applicable
闪点 (°C)
Not applicable