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CAS 183551-51-1

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3,5-BIS(TRIFLUOROMETHYL)BENZYL METHANESULPHONATE

Description:
3,5-Bis(trifluoromethyl)benzyl methanesulfonate is a chemical compound characterized by its unique structure, which includes a benzyl group substituted with two trifluoromethyl groups at the 3 and 5 positions, along with a methanesulfonate functional group. This compound is typically a white to off-white solid and is known for its high reactivity, particularly in nucleophilic substitution reactions due to the presence of the sulfonate group, which is a good leaving group. The trifluoromethyl groups contribute to its lipophilicity and can enhance its biological activity, making it of interest in various fields, including medicinal chemistry and materials science. Additionally, the presence of fluorine atoms often imparts unique electronic properties, which can influence the compound's reactivity and stability. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, 3,5-bis(trifluoromethyl)benzyl methanesulfonate is a versatile compound with significant potential for applications in organic synthesis and pharmaceutical development.
Formula:C10H8F6O3S
InChI:InChI=1/C10H8F6O3S/c1-20(17,18)19-5-6-2-7(9(11,12)13)4-8(3-6)10(14,15)16/h2-4H,5H2,1H3
SMILES:CS(=O)(=O)OCc1cc(cc(c1)C(F)(F)F)C(F)(F)F
Synonyms:
  • 3,5-Bis-Trifluoromethyl-Benzyl-Methansulfonate
  • 3,5-Bis(trifluoromethyl)benzyl methanesulphonate 98%
  • 3,5-Bis(trifluoromethyl)benzylmethanesulphonate98%
  • 3,5-Bis(Trifluoromethyl)Benzyl Methanesulfonate
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