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CAS 1256355-30-2

:

3,5-Difluorobenzyl bromide

Description:
3,5-Difluorobenzyl bromide is an organic compound characterized by the presence of a benzyl group substituted with two fluorine atoms at the 3 and 5 positions and a bromine atom at the benzyl carbon. This compound typically appears as a colorless to pale yellow liquid and is known for its reactivity due to the presence of the bromine atom, which can participate in nucleophilic substitution reactions. The fluorine substituents contribute to the compound's unique electronic properties, influencing its polarity and reactivity. 3,5-Difluorobenzyl bromide is often utilized in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals, due to its ability to serve as an electrophilic building block. It is important to handle this compound with care, as it may pose health risks if inhaled or ingested, and appropriate safety measures should be taken during its use in laboratory settings. Additionally, its environmental impact should be considered, as halogenated compounds can exhibit persistence in the environment.
Formula:C15H3F29O5
InChI:InChI=1/C15H3F29O5/c16-2(1-45,7(22,23)24)46-13(39,40)4(19,9(28,29)30)48-15(43,44)6(21,11(34,35)36)49-14(41,42)5(20,10(31,32)33)47-12(37,38)3(17,18)8(25,26)27/h45H,1H2
SMILES:C(C(C(F)(F)F)(F)OC(C(C(F)(F)F)(F)OC(C(C(F)(F)F)(F)OC(C(C(F)(F)F)(F)OC(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)O
Synonyms:
  • 1-(Brommethyl)-3,5-difluorbenzol
  • 1-(Bromomethyl)-3,5-difluorobenzene
  • 141776-91-2
  • Benzene, 1-(bromomethyl)-3,5-difluoro-
  • Fr Cf E1E
  • 2,4,4,5,7,7,8,10,10,11,13,13,14,14,15,15,15-Heptadecafluoro-2,5,8,11-Tetrakis(Trifluoromethyl)-3,6,9,12-Tetraoxapentadecan-1-Ol
  • 5-Fluoro-2-formylbenzeneboronic acid
  • 5-Fluoro-2-formylphenylboronic acid
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