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CAS 175202-21-8

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N-[3,5-Bis(trifluoromethyl)benzenesulphonyl)-L-methionine methyl ester

Description:
N-[3,5-Bis(trifluoromethyl)benzenesulphonyl)-L-methionine methyl ester is a synthetic compound characterized by its unique structure, which includes a methionine derivative linked to a sulfonyl group with trifluoromethyl substituents. This compound typically exhibits high lipophilicity due to the presence of the trifluoromethyl groups, which can enhance its biological activity and stability. The sulfonyl moiety contributes to its potential as a reactive electrophile, making it useful in various chemical reactions, including those involving nucleophiles. The methyl ester functionality suggests that it may be hydrolyzed to release the corresponding carboxylic acid, which can influence its solubility and reactivity in biological systems. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential interactions with biological targets. However, specific applications and biological activities would require further investigation through empirical studies. Safety and handling precautions should be observed, as with any chemical substance, particularly those with fluorinated groups.
Formula:C13H15F6N3O3S2
InChI:InChI=1/C13H15F6N3O3S2/c1-26-3-2-10(11(23)21-20)22-27(24,25)9-5-7(12(14,15)16)4-8(6-9)13(17,18)19/h4-6,10,22H,2-3,20H2,1H3,(H,21,23)
SMILES:CSCCC(C(=NN)O)NS(=O)(=O)c1cc(cc(c1)C(F)(F)F)C(F)(F)F
Synonyms:
  • Bistrifluoromethylbenzenesulphonylmethioninemethylester
  • Methyl 2-({[3,5-Di(Trifluoromethyl)Phenyl]Sulfonyl}Amino)-4-(Methylthio)Butanoate
  • methyl N-{[3,5-bis(trifluoromethyl)phenyl]sulfonyl}-L-methioninate
  • N-[1-(hydrazinocarbonyl)-3-(methylsulfanyl)propyl]-3,5-bis(trifluoromethyl)benzenesulfonamide (non-preferred name)
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