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Catalog Number:
07409
CAS Number:
268731-06-2
Fmoc-4-(Boc-aminométhyl)-D-phénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-Phe(4-CH2NHBoc)-OH, Fmoc- p -(Boc-aminométhyl)-D-Phe-OH
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$85.60 /250 mg
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Product Information

Fmoc-4-(Boc-aminomethyl)-D-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 with various coupling reactions, making it an ideal choice for researchers focusing on complex peptide structures.

In the pharmaceutical industry, Fmoc-4-(Boc-aminomethyl)-D-phenylalanine is particularly valuable for the synthesis of bioactive peptides, which are crucial in therapeutic applications such as hormone replacement therapies and targeted drug delivery systems. Its unique structure allows for the incorporation of D-amino acids, which can enhance the stability and bioactivity of the resulting peptides. Researchers appreciate its ease of use and the efficiency it brings to peptide synthesis, making it a preferred choice for both academic and industrial applications.

Synonyms
Fmoc-D-Phe(4-CH2NHBoc)-OH, Fmoc- p -(Boc-aminométhyl)-D-Phe-OH
CAS Number
268731-06-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C30H32N2O6
Molecular Weight
516.59
MDL Number
MFCD02094578
PubChem ID
6915687
Appearance
Poudre blanche
Optical Rotation
[a] 25 D = 18 ± 2 ° (C = 1 dans DMF) 20 D = -37 ± 2 ° (C = 1 dans CHCl3)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-D-Phe(4-CH2NHBoc)-OH, Fmoc- p -(Boc-aminométhyl)-D-Phe-OH
CAS Number
268731-06-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C30H32N2O6
Molecular Weight
516.59
MDL Number
MFCD02094578
PubChem ID
6915687
Appearance
Poudre blanche
Optical Rotation
[a] 25 D = 18 ± 2 ° (C = 1 dans DMF) 20 D = -37 ± 2 ° (C = 1 dans CHCl3)
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-aminomethyl)-D-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides efficiently and with high purity.
  • Drug Development: Its unique structure aids in the design of peptide-based drugs, particularly in targeting specific receptors, which can lead to more effective treatments with fewer side effects.
  • Bioconjugation: The compound can be used to attach peptides to other biomolecules, enhancing the functionality of therapeutic agents in targeted drug delivery systems.
  • Research in Neuroscience: It plays a role in studying neuropeptides, contributing to the understanding of neurological pathways and potential treatments for neurodegenerative diseases.
  • Custom Peptide Libraries: This chemical is essential for generating diverse peptide libraries, which are crucial for screening potential drug candidates and discovering new therapeutic targets.

Citations