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CAS 138647-49-1

:

1-(tertbutoxycarbonyl)-1,2,3,6-tetrahydropyridin-4-yltrifluoromethanesulfonate

Description:
1-(tert-Butoxycarbonyl)-1,2,3,6-tetrahydropyridin-4-yltrifluoromethanesulfonate, with CAS number 138647-49-1, is a chemical compound that features a tetrahydropyridine ring substituted with a tert-butoxycarbonyl (Boc) group and a trifluoromethanesulfonate (triflate) moiety. The presence of the Boc group indicates that this compound is likely used as a protecting group in organic synthesis, particularly in the context of amine protection. The triflate group is known for its excellent leaving group ability, making this compound useful in various nucleophilic substitution reactions. The tetrahydropyridine structure contributes to the compound's potential biological activity, as derivatives of tetrahydropyridine are often found in pharmaceuticals. Additionally, the trifluoromethanesulfonate group enhances the compound's reactivity and solubility in polar solvents. Overall, this compound is of interest in synthetic organic chemistry and medicinal chemistry due to its functional groups and structural features that facilitate further chemical transformations.
Formula:C11H16F3NO5S
InChI:InChI=1/C11H16F3NO5S/c1-10(2,3)19-9(16)15-6-4-8(5-7-15)20-21(17,18)11(12,13)14/h4H,5-7H2,1-3H3
SMILES:CC(C)(C)OC(=O)N1CC=C(CC1)OS(=O)(=O)C(F)(F)F
Synonyms:
  • Tert-Butyl 4-(Trifluoromethylsulfonyloxy)-5,6-Dihydropyridine-1(2H)-Carboxylate
  • tert-butyl 4-{[(trifluoromethyl)sulfonyl]oxy}-3,6-dihydropyridine-1(2H)-carboxylate
  • 1-(Tert-Butoxycarbonyl)-1,2,3,6-Tetrahydropyridin-4-Yo Trifluoromethanesulfonate
  • 1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-4-[[(trifluoroMethyl)sulfonyl]oxy]-, 1,1-diMethylethyl ester
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