Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
29641
CAS Number:
173963-91-2
R-Fmoc-2-amino-3-(3-(Boc-amino)-propylsulfanyl)-propionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Cys(3-(Boc-amino)-propyl)-OH
Documents
$100.05 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

(R)-Fmoc-2-amino-3-(3-(Boc-amino)-propylsulfanyl)-propionic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a protective Fmoc group, which facilitates the selective deprotection of amines during solid-phase peptide synthesis, making it an essential building block for researchers in the field of medicinal chemistry. Its unique structure, incorporating a Boc-protected amino group and a sulfanyl moiety, enhances its reactivity and compatibility with various coupling agents, allowing for the efficient assembly of complex peptide sequences.

This compound is particularly beneficial in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its application extends to the synthesis of bioactive peptides, which can serve as potential drug candidates or research tools in the study of biological processes. Researchers appreciate the compound's stability and ease of handling, which streamline the synthesis workflow, ultimately leading to higher yields and purities in peptide production.

Synonyms
Fmoc-L-Cys(3-(Boc-amino)-propyl)-OH
CAS Number
173963-91-2
Purity
≥ 98% (HPLC)
Molecular Formula
C26H32N2O6S
Molecular Weight
500.61
MDL Number
MFCD01318742
PubChem ID
22490534
Appearance
White powder
Optical Rotation
[a]D20 = -31 ± 2º (C=1 in DMF)
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-Cys(3-(Boc-amino)-propyl)-OH
CAS Number
173963-91-2
Purity
≥ 98% (HPLC)
Molecular Formula
C26H32N2O6S
Molecular Weight
500.61
MDL Number
MFCD01318742
PubChem ID
22490534
Appearance
White powder
Optical Rotation
[a]D20 = -31 ± 2º (C=1 in DMF)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R)-Fmoc-2-amino-3-(3-(Boc-amino)-propylsulfanyl)-propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex peptides with specific functionalities.
  • Drug Development: Its unique structure makes it valuable in medicinal chemistry for developing novel therapeutics, particularly in targeting specific biological pathways.
  • Bioconjugation: The compound can be used to create bioconjugates, enhancing the delivery of drugs or imaging agents to specific cells or tissues, which is crucial in targeted therapy.
  • Research in Protein Engineering: It aids in the modification of proteins, allowing researchers to study protein interactions and functions more effectively, which is essential in biotechnology and pharmaceutical research.
  • Development of Diagnostic Tools: Its properties enable the design of sensitive assays for detecting biomolecules, contributing to advancements in diagnostics and personalized medicine.

Citations