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Catalog Number:
31704
CAS Number:
864876-97-1
Fmoc-L-Thr(tBu)-O-CH2-Ph-OCH2-CH2-COOH
Purity:
≥ 98% (HPLC)
Documents
$155.00 /100MG
Pack Size Availability Price
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Product Information

Fmoc-L-Thr(tBu)-O-CH2-Ph-OCH2-CH2-COOH 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 unique structure, including a t-butyl (tBu) side chain, enhances its stability and solubility, making it an excellent choice for researchers looking to create complex peptides with high purity and yield.

In the pharmaceutical industry, this compound plays a crucial role in the development of therapeutic peptides, particularly those targeting specific biological pathways. Its ability to facilitate the synthesis of modified peptides allows for the exploration of new drug candidates with improved efficacy and reduced side effects. Additionally, Fmoc-L-Thr(tBu)-O-CH2-Ph-OCH2-CH2-COOH is recognized for its compatibility with various coupling reagents, making it a preferred choice for chemists aiming to streamline their synthesis processes.

CAS Number
864876-97-1
Purity
≥ 98% (HPLC)
Molecular Formula
C33H37NO8
Molecular Weight
575.66
MDL Number
MFCD08457854
PubChem ID
155893426
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
CAS Number
864876-97-1
Purity
≥ 98% (HPLC)
Molecular Formula
C33H37NO8
Molecular Weight
575.66
MDL Number
MFCD08457854
PubChem ID
155893426
Appearance
White powder
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-L-Thr(tBu)-O-CH2-Ph-OCH2-CH2-COOH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, enabling researchers to create complex molecules for drug development and biological studies.
  • Drug Delivery Systems: Its unique structure allows for the formulation of advanced drug delivery systems, improving the bioavailability and efficacy of therapeutic agents.
  • Bioconjugation: The compound is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in diagnostics and therapeutic applications.
  • Research in Cancer Therapy: It plays a role in developing targeted therapies for cancer, where its properties help in designing compounds that can selectively deliver drugs to tumor cells.
  • Protein Engineering: The compound is valuable in protein engineering, aiding in the modification of proteins to enhance their stability and functionality for various industrial and medical applications.

Citations