🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
16860
CAS Number:
1213080-68-2
Boc-3-(Fmoc-aminométhyl)-D-phénylalanine
Purity:
≥ 99 % (pureté chirale)
Synonym(s):
Boc-D-Phe(3-CH2NHFmoc)-OH, Boc- m -(Fmoc-aminométhyl)-D-Phe-OH
Documents
$86.23 /250 mg
Taille
Request Bulk Quote
Product Information

Boc-3-(Fmoc-aminomethyl)-D-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique combination of protective groups, namely the Boc (tert-butyloxycarbonyl) and Fmoc (9-fluorenylmethyloxycarbonyl), which facilitate selective reactions and enhance the stability of peptides during synthesis. Its structure allows for efficient incorporation into peptides, making it an essential building block for researchers in the fields of medicinal chemistry and biochemistry.

In practical applications, Boc-3-(Fmoc-aminomethyl)-D-phenylalanine is particularly valuable in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its ability to protect functional groups while allowing for further modifications makes it an ideal choice for synthesizing complex peptide structures. Additionally, this compound can be employed in the design of targeted drug delivery systems, enhancing the efficacy of therapeutic agents. Researchers and industry professionals will appreciate its reliability and effectiveness in advancing their projects.

Synonyms
Boc-D-Phe(3-CH2NHFmoc)-OH, Boc- m -(Fmoc-aminométhyl)-D-Phe-OH
CAS Number
1213080-68-2
Purity
≥ 99 % (pureté chirale)
Molecular Formula
C30H32N2O6
Molecular Weight
516.58
MDL Number
MFCD06659123
PubChem ID
53398427
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = +12 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-D-Phe(3-CH2NHFmoc)-OH, Boc- m -(Fmoc-aminométhyl)-D-Phe-OH
CAS Number
1213080-68-2
Purity
≥ 99 % (pureté chirale)
Molecular Formula
C30H32N2O6
Molecular Weight
516.58
MDL Number
MFCD06659123
PubChem ID
53398427
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = +12 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-3-(Fmoc-aminomethyl)-D-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of therapeutic agents and research tools in biochemistry.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for designing and optimizing drug candidates, especially those targeting specific receptors or enzymes.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to drugs or imaging agents, enhancing their efficacy and targeting capabilities.
  • Protein Engineering: It aids in the modification of proteins, enabling scientists to create variants with improved stability or activity, which is vital in fields like enzyme technology and vaccine development.
  • Research in Neuroscience: The compound is utilized in studies related to neuropeptides, facilitating the exploration of their roles in neurological functions and potential treatments for neurological disorders.

Citations