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Catalog Number:
22656
CAS Number:
1013883-02-7
Fmoc-4-[2-(Boc-amino)ethoxy]-L-phenylalanine
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-4-[2-(Boc-amino)ethoxy]-L-Phe-OH
Documents
$130.00 /100MG
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Product Information

Fmoc-4-[2-(Boc-amino)ethoxy]-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 utility, allowing for the protection of amines in complex synthetic pathways. Researchers and industry professionals appreciate its stability and compatibility with various coupling reagents, making it an ideal choice for constructing peptides with specific sequences and functionalities.

This compound is particularly valuable in the pharmaceutical industry, where it is employed in the synthesis of bioactive peptides and therapeutic agents. Its unique structure allows for the incorporation of diverse functional groups, facilitating the design of peptides with enhanced biological activity. Additionally, Fmoc-4-[2-(Boc-amino)ethoxy]-L-phenylalanine can be utilized in the development of targeted drug delivery systems, providing a platform for creating innovative therapeutics. Its robust performance in peptide synthesis positions it as a preferred choice for researchers aiming to streamline their workflows and achieve high yields in peptide production.

Synonyms
Fmoc-4-[2-(Boc-amino)ethoxy]-L-Phe-OH
CAS Number
1013883-02-7
Purity
≥ 97% (HPLC)
Molecular Formula
C31H34N2O7
Molecular Weight
546.62
MDL Number
MFCD07781260
PubChem ID
4712598
Appearance
White powder
Optical Rotation
[a]D20 = -16 ± 3 º (C=1 in DMF)
Conditions
Store at ≤ -4 °C
General Information
Synonyms
Fmoc-4-[2-(Boc-amino)ethoxy]-L-Phe-OH
CAS Number
1013883-02-7
Purity
≥ 97% (HPLC)
Molecular Formula
C31H34N2O7
Molecular Weight
546.62
MDL Number
MFCD07781260
PubChem ID
4712598
Appearance
White powder
Optical Rotation
[a]D20 = -16 ± 3 º (C=1 in DMF)
Conditions
Store at ≤ -4 °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-[2-(Boc-amino)ethoxy]-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for drug development and biological studies.
  • Drug Design: Its unique properties enable the design of novel therapeutic agents, particularly in the fields of oncology and neurology, where targeted therapies are crucial.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of biomolecules to drugs, enhancing their efficacy and specificity.
  • Material Science: In the development of smart materials, it contributes to the creation of responsive systems that can change properties under specific conditions, useful in sensors and actuators.
  • Research in Protein Engineering: It plays a significant role in modifying proteins to study their functions, helping scientists understand disease mechanisms and develop new treatments.

Citations