CAS 141776-91-2: 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 a versatile building block. It is important to handle this compound with care, as it may pose health risks, including irritation to the skin and eyes, and should be used in a well-ventilated area with appropriate personal protective equipment. As with many halogenated compounds, environmental considerations regarding its disposal and potential toxicity should also be taken into account.
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
- 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
