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Catalog Number:
15063
CAS Number:
141743-30-8
Sel de dicyclohexylammonium de Fmoc- N- (2- tert -butoxyéthyl)glycine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-Nhser(tBu)-OH·DCHA
Documents
$40.00 /100 mg
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Product Information

Fmoc-N-(2-tert-butoxyethyl)glycine dicyclohexylammonium salt is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which is essential for the selective protection of amino acids during solid-phase peptide synthesis. Its unique structure, incorporating a tert-butoxyethyl side chain, enhances solubility and stability, making it an ideal choice for researchers working on complex peptide sequences.

In addition to its role in peptide synthesis, this compound is particularly valuable in the pharmaceutical industry for developing novel therapeutics. Its dicyclohexylammonium salt form improves the compound's handling and solubility in various solvents, facilitating easier processing and formulation. Researchers have found it beneficial in applications ranging from drug delivery systems to the synthesis of biologically active peptides, showcasing its potential to streamline workflows and enhance product outcomes in both academic and industrial settings.

Synonyms
Fmoc-Nhser(tBu)-OH·DCHA
CAS Number
141743-30-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 23 H 27 NO 5 · C 12 H 23 N
Molecular Weight
578.67
MDL Number
MFCD08236869
PubChem ID
2756166
Melting Point
113-118 °C
Appearance
Poudre cristalline blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-Nhser(tBu)-OH·DCHA
CAS Number
141743-30-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 23 H 27 NO 5 · C 12 H 23 N
Molecular Weight
578.67
MDL Number
MFCD08236869
PubChem ID
2756166
Melting Point
113-118 °C
Appearance
Poudre cristalline blanche
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-N-(2-tert-butoxyethyl)glycine dicyclohexylammonium salt is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It is instrumental in the design of peptide-based pharmaceuticals, enhancing the stability and bioavailability of therapeutic agents.
  • Bioconjugation: The compound is used in the conjugation of peptides to biomolecules, facilitating the creation of targeted drug delivery systems.
  • Research in Neuroscience: It aids in the synthesis of neuropeptides, which are crucial for studying neurological functions and disorders.
  • Analytical Chemistry: This chemical is employed in the development of analytical methods for peptide characterization, improving the accuracy of mass spectrometry and chromatography techniques.

Citations