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

Catalog Number:
29637
CAS Number:
685863-48-3
R-Fmoc-2-amino-3-(2-tert-butoxycarbonyl-ethylsulfanyl)-propionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Cys(tert-butoxycarbonylethyl)-OH
Documents
$106.96 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

(R)-Fmoc-2-amino-3-(2-tert-butoxycarbonyl-ethylsulfanyl)-propionic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, incorporating a tert-butoxycarbonyl group and a sulfanyl moiety, enhances its stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry.

This compound is particularly valuable in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its application extends to the synthesis of complex peptides that can be used in various biological assays, drug discovery, and the development of novel therapeutic agents. The ability to easily manipulate its structure allows for the exploration of diverse chemical properties, making it a preferred choice for professionals seeking reliable and efficient solutions in peptide synthesis.

Synonyms
Fmoc-L-Cys(tert-butoxycarbonylethyl)-OH
CAS Number
685863-48-3
Purity
≥ 98% (HPLC)
Molecular Formula
C25H29NO6S
Molecular Weight
471.57
MDL Number
MFCD18782825
PubChem ID
138108396
Appearance
White powder
Optical Rotation
[a]D20 = -28.3 ± 2º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-Cys(tert-butoxycarbonylethyl)-OH
CAS Number
685863-48-3
Purity
≥ 98% (HPLC)
Molecular Formula
C25H29NO6S
Molecular Weight
471.57
MDL Number
MFCD18782825
PubChem ID
138108396
Appearance
White powder
Optical Rotation
[a]D20 = -28.3 ± 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-(2-tert-butoxycarbonyl-ethylsulfanyl)-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 (SPPS), allowing for the creation of complex peptide sequences with high purity.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for developing peptide-based drugs, offering a pathway to create therapeutics with enhanced efficacy and specificity.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of peptides to other biomolecules, which is essential for creating targeted drug delivery systems.
  • Research in Protein Engineering: It aids researchers in modifying proteins to study their functions and interactions, contributing to advancements in biotechnology and molecular biology.
  • Diagnostic Applications: The compound can be utilized in the development of diagnostic tools, particularly in assays that require specific peptide interactions, enhancing the sensitivity and accuracy of tests.

Citations