
CAS 955946-10-8
:4-nitro-2-(trifluoromethoxy)benzyl bromide
Description:
4-Nitro-2-(trifluoromethoxy)benzyl bromide is an organic compound characterized by its aromatic structure, which includes a nitro group and a trifluoromethoxy substituent on a benzyl ring. The presence of the nitro group typically imparts electron-withdrawing properties, influencing the compound's reactivity and polarity. The trifluoromethoxy group enhances the compound's lipophilicity and can affect its solubility in various solvents. As a bromide, it serves as a potential electrophile in nucleophilic substitution reactions, making it useful in synthetic organic chemistry. The compound's molecular structure suggests it may exhibit interesting biological activity, although specific biological properties would require further investigation. Additionally, the presence of fluorine atoms often contributes to unique physical and chemical properties, such as increased stability and altered reactivity. Overall, 4-nitro-2-(trifluoromethoxy)benzyl bromide is a versatile compound with potential applications in pharmaceuticals and materials science, though safety and handling precautions should be observed due to the presence of bromine and nitro functionalities.
Formula:C8H5Br2F3O
InChI:InChI=1S/C8H5Br2F3O/c9-4-5-1-2-6(10)3-7(5)14-8(11,12)13/h1-3H,4H2
InChI key:FDAOMROLPVEVGJ-UHFFFAOYSA-N
SMILES:C1=CC(=C(C=C1Br)OC(F)(F)F)CBr
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4-Bromo-2-(trifluoromethoxy)benzyl bromide
CAS:4-Bromo-2-(trifluoromethoxy)benzyl bromideFormula:C8H5Br2F3OPurity:≥95%Molecular weight:333.9279

