structure of t-Butyl N-Cbz-DL-PhenylalaninaMide

t-Butyl N-Cbz-DL-PhenylalaninaMide

CAS No.: 4124-61-2
M. Wt: 354.44300
M. Fa: C21H26N2O3
InChI Key: -

Names and Identifiers of t-Butyl N-Cbz-DL-PhenylalaninaMide

CAS Number

4124-61-2

IUPAC Name

(phenylmethyl) N-[1-(tert-butylamino)-1-oxidanylidene-3-phenyl-propan-2-yl]carbamate

Canonical SMILES

CC(C)(C)NC(=O)C(CC1=CC=CC=C1)NC(=O)OCC2=CC=CC=C2

Physical and chemical properties of t-Butyl N-Cbz-DL-PhenylalaninaMide

Exact Mass

354.19400

LogP

4.22060

Molecular Formula

C21H26N2O3

Molecular Weight

354.44300

PSA

67.43000

Applications of t-Butyl N-Cbz-DL-PhenylalaninaMide

T-Butyl N-cbz-DL-phenylalaninamide finds applications in various fields:

  • Pharmaceuticals: Used as an intermediate in the synthesis of peptide-based drugs.
  • Biotechnology: Serves as a building block for designing novel peptides with specific biological activities.
  • Research: Employed in studies focusing on enzyme catalysis and peptide synthesis methodologies.

Interaction Studies of t-Butyl N-Cbz-DL-PhenylalaninaMide

Interaction studies involving T-butyl N-cbz-DL-phenylalaninamide often focus on its reactivity with various catalysts and enzymes. Research has shown that its structural features allow for selective interactions that are crucial in enzymatic reactions. The presence of the Cbz group influences the compound's solubility and reactivity, affecting its interaction with biological targets. Furthermore, studies on its derivatives have highlighted potential interactions with receptors involved in neurotransmission.

Biological Activity of t-Butyl N-Cbz-DL-PhenylalaninaMide

The biological activity of T-butyl N-cbz-DL-phenylalaninamide is primarily linked to its role as a precursor in peptide synthesis. Compounds derived from this structure have been investigated for their potential therapeutic effects, including antimicrobial and anticancer activities. The Cbz protecting group enhances stability and solubility, making it suitable for various biological applications. Research indicates that derivatives of phenylalanine exhibit neuroprotective properties and may influence neurotransmitter levels.

Retrosynthesis analysis of t-Butyl N-Cbz-DL-PhenylalaninaMide

  • Route#1

    Cas:3397-32-8
    Cas:75-64-9
    Cas:4124-61-2
  • Route#2

    Cas:75-64-9
    Cas:4124-61-2