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Catalog Number:
03755
CAS Number:
174132-31-1
Fmoc-4-(Boc-amino)-L-phénylalanine
Purity:
≥ 97 % (dosage)
Synonym(s):
Fmoc-L-Phe(4-NHBoc)-OH, Fmoc- p- (Boc-amino)-L-Phe-OH, Fmoc-Phe(4-NHBoc)-OH
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Product Information

Fmoc-4-(Boc-amino)-L-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during solid-phase peptide synthesis. Its Boc (tert-butyloxycarbonyl) group further enhances its stability and compatibility in various synthetic pathways, making it an ideal choice for researchers in the fields of biochemistry and medicinal chemistry.

The unique structure of Fmoc-4-(Boc-amino)-L-phenylalanine allows for the efficient assembly of complex peptides, facilitating the exploration of novel therapeutic agents. Its application extends to the synthesis of peptide-based drugs, where precise control over amino acid sequences is crucial. Additionally, this compound can be employed in the development of biomaterials and drug delivery systems, showcasing its potential in advancing pharmaceutical formulations. With its robust properties and practical applications, Fmoc-4-(Boc-amino)-L-phenylalanine stands out as a valuable tool for researchers aiming to innovate in peptide chemistry.

Synonyms
Fmoc-L-Phe(4-NHBoc)-OH, Fmoc- p- (Boc-amino)-L-Phe-OH, Fmoc-Phe(4-NHBoc)-OH
CAS Number
174132-31-1
Purity
≥ 97 % (dosage)
Molecular Formula
C29H30N2O6
Molecular Weight
502.6
MDL Number
MFCD00237007
PubChem ID
4712562
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-L-Phe(4-NHBoc)-OH, Fmoc- p- (Boc-amino)-L-Phe-OH, Fmoc-Phe(4-NHBoc)-OH
CAS Number
174132-31-1
Purity
≥ 97 % (dosage)
Molecular Formula
C29H30N2O6
Molecular Weight
502.6
MDL Number
MFCD00237007
PubChem ID
4712562
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-4-(Boc-amino)-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound is a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides efficiently. Its protective groups facilitate selective reactions, making it easier to manipulate the peptide chain.
  • Drug Development: In pharmaceutical research, it serves as an important intermediate for synthesizing bioactive peptides, which can lead to the development of new therapeutic agents targeting various diseases.
  • Bioconjugation: The compound is used in bioconjugation processes to attach peptides to other biomolecules, enhancing the efficacy of drug delivery systems and improving the targeting of therapeutic agents.
  • Protein Engineering: It plays a significant role in modifying proteins to study structure-function relationships, helping researchers understand how changes in amino acid sequences affect protein behavior.
  • Academic Research: In educational settings, it is commonly employed in laboratories for teaching peptide synthesis techniques, providing students with hands-on experience in organic chemistry and biochemistry.

Citations