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Catalog Number:
07408
CAS Number:
204715-91-3
Fmoc-4-(Boc-aminometil)-L-fenilalanina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Phe(4-CH2NHBoc)-OH, Fmoc- p -(Boc-aminometil)-L-Phe-OH, Fmoc-Phe(4-CH2NHBoc)-OH
Documents
$85.60 /250 mg
Tamaño
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Product Information

Fmoc-4-(Boc-aminomethyl)-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 the synthesis of peptides. The Boc (tert-butyloxycarbonyl) group further enhances its stability and solubility, making it an ideal choice for solid-phase peptide synthesis (SPPS). Researchers and industry professionals appreciate its ability to facilitate the formation of complex peptides with high purity and yield, which is crucial in pharmaceutical applications.

In addition to its role in peptide synthesis, Fmoc-4-(Boc-aminomethyl)-L-phenylalanine is also valuable in the development of therapeutic agents and biologically active compounds. Its unique structure allows for the incorporation of various functional groups, enabling the design of tailored peptides for specific biological activities. This compound stands out due to its ease of use and compatibility with various coupling reagents, making it a preferred choice for chemists looking to streamline their synthesis processes while achieving optimal results.

Synonyms
Fmoc-L-Phe(4-CH2NHBoc)-OH, Fmoc- p -(Boc-aminometil)-L-Phe-OH, Fmoc-Phe(4-CH2NHBoc)-OH
CAS Number
204715-91-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C30H32N2O6
Molecular Weight
516.59
MDL Number
MFCD01317015
PubChem ID
6915687
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -19 ± 2 º (C=1 en DMF) D 25 = 40 ± 2 º (C=1 en CHCl3)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-Phe(4-CH2NHBoc)-OH, Fmoc- p -(Boc-aminometil)-L-Phe-OH, Fmoc-Phe(4-CH2NHBoc)-OH
CAS Number
204715-91-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C30H32N2O6
Molecular Weight
516.59
MDL Number
MFCD01317015
PubChem ID
6915687
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -19 ± 2 º (C=1 en DMF) D 25 = 40 ± 2 º (C=1 en CHCl3)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Peptide Synthesis: This compound is a key building block in the synthesis of peptides, allowing researchers to create custom sequences for various applications in drug development and biological research.
  • Drug Development: Its unique structure aids in the design of peptide-based therapeutics, particularly in targeting specific biological pathways, enhancing the efficacy of new medications.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking peptides to other molecules, such as drugs or imaging agents, which is crucial for developing targeted therapies.
  • Research in Cancer Therapeutics: It plays a role in the development of peptide inhibitors that can selectively target cancer cells, contributing to more effective cancer treatments with fewer side effects.
  • Protein Engineering: This chemical is valuable in modifying proteins to study their functions and interactions, providing insights that can lead to advancements in biotechnology and synthetic biology.

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