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CAS 170462-69-8

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N-[(1,1-Dimethylethoxy)carbonyl]-2-(trifluoromethyl)leucine

Description:
N-[(1,1-Dimethylethoxy)carbonyl]-2-(trifluoromethyl)leucine, with CAS number 170462-69-8, is an amino acid derivative characterized by the presence of a trifluoromethyl group and a dimethylethoxycarbonyl protecting group. This compound is typically used in peptide synthesis and medicinal chemistry due to its unique structural features that enhance its reactivity and stability. The trifluoromethyl group contributes to increased lipophilicity and can influence the biological activity of the molecule, making it a valuable component in drug design. The dimethylethoxycarbonyl group serves as a protective moiety, allowing for selective reactions during synthesis while preventing unwanted side reactions. This compound is generally solid at room temperature and is soluble in organic solvents, which facilitates its use in various chemical reactions. Its specific properties, such as melting point, boiling point, and spectral characteristics, can vary based on purity and environmental conditions, but it is primarily recognized for its role in the synthesis of more complex molecules in pharmaceutical applications.
Formula:C12H20F3NO4
InChI:InChI=1S/C12H20F3NO4/c1-7(2)6-11(8(17)18,12(13,14)15)16-9(19)20-10(3,4)5/h7H,6H2,1-5H3,(H,16,19)(H,17,18)
InChI key:InChIKey=MUJOGMJYEGHPQF-UHFFFAOYSA-N
SMILES:C(NC(OC(C)(C)C)=O)(CC(C)C)(C(F)(F)F)C(O)=O
Synonyms:
  • N-[(1,1-Dimethylethoxy)carbonyl]-2-(trifluoromethyl)leucine
  • Leucine, N-[(1,1-dimethylethoxy)carbonyl]-2-(trifluoromethyl)-
  • 2-[[(tert-Butoxy)carbonyl]amino]-4-methyl-2-(trifluoromethyl)pentanoic acid
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