🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
29643
CAS Number:
866602-35-9
S-Fmoc-2-amino-6-(Boc-tert-butoxycarbonylmethyl-amino)-hexanoic acid
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-CML(OtBu)(Boc)-OH
Documents
$234.85 /25MG
Pack Size Availability Price
Request Bulk Quote
Product Information

(S)-Fmoc-2-amino-6-(Boc-tert-butoxycarbonylmethyl-amino)-hexanoic acid 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 Boc (tert-butoxycarbonyl) group further enhances its stability and solubility, making it an ideal choice for researchers looking to streamline their synthetic processes.

In the pharmaceutical industry, (S)-Fmoc-2-amino-6-(Boc-tert-butoxycarbonylmethyl-amino)-hexanoic acid plays a crucial role in the development of biologically active peptides, which are increasingly important in therapeutic applications. Its unique structure allows for the incorporation of diverse functionalities, enabling the design of peptides with tailored properties for specific biological activities. Researchers benefit from its ease of use and compatibility with various coupling reagents, facilitating efficient synthesis and purification of target compounds.

Synonyms
Fmoc-CML(OtBu)(Boc)-OH
CAS Number
866602-35-9
Purity
≥ 97% (HPLC)
Molecular Formula
C32H42N2O8
Molecular Weight
582.69
MDL Number
MFCD11226791
PubChem ID
75110600
Melting Point
55-72 ºc
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-CML(OtBu)(Boc)-OH
CAS Number
866602-35-9
Purity
≥ 97% (HPLC)
Molecular Formula
C32H42N2O8
Molecular Weight
582.69
MDL Number
MFCD11226791
PubChem ID
75110600
Melting Point
55-72 ºc
Appearance
White powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-Fmoc-2-amino-6-(Boc-tert-butoxycarbonylmethyl-amino)-hexanoic acid 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 Development: Its unique structure enhances the solubility and stability of peptide-based drugs, making it a valuable component in pharmaceutical formulations.
  • Bioconjugation: The compound is used in bioconjugation techniques, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted therapies.
  • Research in Neuroscience: It plays a role in developing neuropeptides, which are important for understanding neurological functions and potential treatments for disorders.
  • Custom Synthesis Services: Many laboratories utilize this compound in custom synthesis services, providing tailored solutions for specific research needs in various scientific fields.

Citations