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

Catalog Number:
14834
CAS Number:
313052-20-9
Ácido S -3-(4-Boc-piperazin-1-il)-2-(Fmoc-amino)propiónico
Purity:
≥ 99 % (TLC)
Synonym(s):
Fmoc-β-(1-piperazinil)-L-Ala(Boc)-OH
Documents
$338.01 /25 mg
Tamaño
Request Bulk Quote
Product Information

(S)-3-(4-Boc-piperazin-1-yl)-2-(Fmoc-amino)propionic acid is a versatile compound widely utilized in the fields of medicinal chemistry and peptide synthesis. This compound features a unique structure that combines a piperazine moiety with a fluorenylmethoxycarbonyl (Fmoc) protecting group, making it an ideal candidate for the development of peptide-based therapeutics. Its Boc (tert-butyloxycarbonyl) group enhances its stability and solubility, facilitating its use in various chemical reactions. Researchers often leverage this compound for the synthesis of complex peptides, which are critical in drug discovery and development, particularly in targeting specific biological pathways.

This compound stands out due to its ability to provide a robust framework for the introduction of diverse amino acids, allowing for the creation of tailored peptides with enhanced biological activity. Its applications extend to the pharmaceutical industry, where it plays a crucial role in the design of novel drug candidates. Additionally, its favorable properties make it a preferred choice for researchers looking to optimize peptide synthesis processes, thereby accelerating the development of innovative therapeutic solutions.

Synonyms
Fmoc-β-(1-piperazinil)-L-Ala(Boc)-OH
CAS Number
313052-20-9
Purity
≥ 99 % (TLC)
Molecular Formula
C27H33N3O6
Molecular Weight
495.58
MDL Number
MFCD01860747
PubChem ID
53421227
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-β-(1-piperazinil)-L-Ala(Boc)-OH
CAS Number
313052-20-9
Purity
≥ 99 % (TLC)
Molecular Formula
C27H33N3O6
Molecular Weight
495.58
MDL Number
MFCD01860747
PubChem ID
53421227
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-3-(4-Boc-piperazin-1-yl)-2-(Fmoc-amino)propionic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, enabling researchers to create specific sequences for therapeutic applications.
  • Drug Development: It plays a crucial role in the development of new pharmaceuticals, particularly in designing compounds that can effectively target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing for the attachment of drugs to antibodies or other biomolecules, enhancing targeted delivery systems.
  • Research in Neuroscience: Its properties make it valuable in studying neurotransmitter systems, aiding in the development of treatments for neurological disorders.
  • Custom Synthesis Services: Many chemical suppliers offer custom synthesis services using this compound, catering to specific research needs and accelerating project timelines.

Citas