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Catalog Number:
22675
CAS Number:
929101-56-4
2S,3S)-Fmoc-Mpc(Trt)-OH
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ácido (2S,4S)-Fmoc-4-tritilmercapto-pirrolidin-2-carboxílico
Documents
$141.41 /25 mg
Tamaño
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Product Information

The compound (2S,3S)-Fmoc-Mpc(Trt)-OH is a versatile building block widely utilized in peptide synthesis and drug development. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which is essential for the selective protection of amines during synthesis. Its trityl (Trt) group enhances stability and solubility, making it an ideal choice for complex peptide sequences. Researchers appreciate its ability to facilitate the synthesis of peptides with high purity and yield, which is crucial in pharmaceutical applications, particularly in the development of therapeutic peptides and proteins.

In addition to its role in peptide synthesis, (2S,3S)-Fmoc-Mpc(Trt)-OH is also employed in various research applications, including the study of protein interactions and the development of novel biomaterials. Its unique structural features allow for the incorporation of diverse functional groups, enabling the design of tailored compounds for specific biological activities. This compound stands out for its efficiency and reliability, making it a preferred choice among professionals in the fields of medicinal chemistry and biochemistry.

Synonyms
Ácido (2S,4S)-Fmoc-4-tritilmercapto-pirrolidin-2-carboxílico
CAS Number
929101-56-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C39H33NO4S
Molecular Weight
611.76
MDL Number
MFCD08457840
PubChem ID
53395530
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -38 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido (2S,4S)-Fmoc-4-tritilmercapto-pirrolidin-2-carboxílico
CAS Number
929101-56-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C39H33NO4S
Molecular Weight
611.76
MDL Number
MFCD08457840
PubChem ID
53395530
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -38 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(2S,3S)-Fmoc-Mpc(Trt)-OH 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 and diverse peptide sequences.
  • Drug Development: It plays a crucial role in drug discovery by facilitating the design of peptide-based therapeutics, which can target specific biological pathways with high precision.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps to attach peptides to other biomolecules, enhancing the efficacy of targeted drug delivery systems.
  • Research in Proteomics: Researchers utilize this chemical in proteomics studies to modify proteins, aiding in the analysis of protein interactions and functions in various biological systems.
  • Custom Synthesis Services: Many chemical suppliers offer custom synthesis services using this compound, providing tailored solutions for researchers needing specific peptide sequences for their studies.

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