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Catalog Number:
22657
CAS Number:
181951-92-8
Fmoc-4-(tert-butoxycarbonylmethoxy)-L-phenylalanine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-4-(tert-butoxycarbonylmethoxy)-L-Phe-OH
Documents
$95.00 /100MG
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Product Information

Fmoc-4-(tert-butoxycarbonylmethoxy)-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. Its unique structure allows for enhanced stability and solubility, making it an ideal choice for researchers in the fields of biochemistry and medicinal chemistry.

This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it facilitates the efficient assembly of complex peptide sequences. Its tert-butoxycarbonylmethoxy group enhances the compound's reactivity and compatibility with various coupling reagents, streamlining the synthesis process. Researchers can leverage Fmoc-4-(tert-butoxycarbonylmethoxy)-L-phenylalanine to create peptides with specific biological activities, paving the way for advancements in therapeutic agents and biomolecular research. With its robust performance and reliability, this compound stands out as a preferred choice for professionals aiming to innovate in peptide-based applications.

Synonyms
Fmoc-4-(tert-butoxycarbonylmethoxy)-L-Phe-OH
CAS Number
181951-92-8
Purity
≥ 98% (HPLC)
Molecular Formula
C30H31NO7
Molecular Weight
517.58
MDL Number
MFCD07781259
PubChem ID
4712597
Appearance
White solid/powder
Optical Rotation
[a]D20 = -17 ± 4 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-4-(tert-butoxycarbonylmethoxy)-L-Phe-OH
CAS Number
181951-92-8
Purity
≥ 98% (HPLC)
Molecular Formula
C30H31NO7
Molecular Weight
517.58
MDL Number
MFCD07781259
PubChem ID
4712597
Appearance
White solid/powder
Optical Rotation
[a]D20 = -17 ± 4 º (C=1 in DMF)
Conditions
Store at 0 - 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-(tert-butoxycarbonylmethoxy)-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 various biological studies.
  • Drug Development: It plays a significant role in the pharmaceutical industry, particularly in the development of peptide-based drugs, which can offer targeted therapies with fewer side effects.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to drugs or imaging agents, enhancing their effectiveness in diagnostics and therapeutics.
  • Research in Cancer Therapy: Its application in creating peptide analogs has shown promise in developing treatments for cancer, providing new avenues for targeted therapies.
  • Protein Engineering: This chemical is essential in protein engineering, helping scientists modify proteins for improved stability and functionality in various applications, including industrial enzymes.

Citations