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Catalog Number:
07053
CAS Number:
173963-91-2
Fmoc-L-Cys(3-(Boc-amino)-propyl)-OH
Purity:
≥ 98% (HPLC)
Synonym(s):
(R)-Fmoc-2-amino-3-(3-(Boc-amino)-propylsulfanyl)-propionic acid
Documents
$125.06 /100MG
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Product Information

Fmoc-L-Cys(3-(Boc-amino)-propyl)-OH 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
(R)-Fmoc-2-amino-3-(3-(Boc-amino)-propylsulfanyl)-propionic acid
CAS Number
173963-91-2
Purity
≥ 98% (HPLC)
Molecular Formula
C26H32N2O6S
Molecular Weight
500.62
MDL Number
MFCD01318742
PubChem ID
22490534
Melting Point
115-119 ºC
Appearance
White powder
Optical Rotation
[a]D24 = -29.0 ± 2º (C=1 in Dimethylformamide)
Conditions
Store at 0-8 °C
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
General Information
Synonyms
(R)-Fmoc-2-amino-3-(3-(Boc-amino)-propylsulfanyl)-propionic acid
CAS Number
173963-91-2
Purity
≥ 98% (HPLC)
Molecular Formula
C26H32N2O6S
Molecular Weight
500.62
MDL Number
MFCD01318742
PubChem ID
22490534
Melting Point
115-119 ºC
Appearance
White powder
Optical Rotation
[a]D24 = -29.0 ± 2º (C=1 in Dimethylformamide)
Conditions
Store at 0-8 °C
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Properties
Additional property information coming soon!
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Applications

Fmoc-S-Boc-3-aminopropyl-L-cysteine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a versatile building block in the synthesis of peptides, particularly in the development of therapeutic proteins and biologics.
  • Drug Development: It is used in the design of novel drug candidates, especially those targeting specific biological pathways, enhancing the efficacy of pharmaceutical formulations.
  • Bioconjugation: The compound facilitates the conjugation of biomolecules, allowing researchers to create targeted delivery systems for drugs and imaging agents.
  • Research in Cancer Therapy: Its unique properties enable the development of targeted therapies that can selectively attack cancer cells, improving treatment outcomes.
  • Protein Engineering: This chemical is essential in modifying proteins to enhance their stability and functionality, which is crucial in various biotechnological applications.

Citations