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

Catalog Number:
35207
CAS Number:
1068435-19-7
Ácido N -Fmoc-2-amino-2-(4-pentenil)-6-heptenoico
Purity:
≥ 99 % (HPLC)
Documents
$325.09 /250 mg
Tamaño
Request Bulk Quote
Product Information

N-Fmoc-2-Amino-2-(4-pentenyl)-6-heptenoic acid is a versatile compound widely utilized in the fields of organic synthesis and peptide chemistry. This amino acid derivative features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, making it an ideal choice for solid-phase peptide synthesis. Its unique structure, which includes a pentenyl side chain, enhances its reactivity and allows for the incorporation of diverse functionalities into peptides, facilitating the development of novel therapeutic agents. Researchers appreciate its stability under various conditions, which is crucial for maintaining the integrity of sensitive peptide sequences during synthesis.

In addition to its role in peptide synthesis, N-Fmoc-2-Amino-2-(4-pentenyl)-6-heptenoic acid can be employed in the development of bioactive compounds and drug discovery. Its ability to form stable linkages with other molecules opens avenues for creating complex structures with potential applications in pharmaceuticals and biotechnology. The compound's unique properties make it a valuable tool for researchers aiming to innovate in the fields of medicinal chemistry and materials science.

CAS Number
1068435-19-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C 27 H 31 N.º 4
Molecular Weight
433.54
MDL Number
MFCD12925762
PubChem ID
50851124
Appearance
Polvo de color blanco a blanquecino
Conditions
Tienda en RT
General Information
CAS Number
1068435-19-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C 27 H 31 N.º 4
Molecular Weight
433.54
MDL Number
MFCD12925762
PubChem ID
50851124
Appearance
Polvo de color blanco a blanquecino
Conditions
Tienda en RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

N-Fmoc-2-Amino-2-(4-pentenyl)-6-heptenoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing researchers to selectively modify amino acids without affecting other functional groups. Its stability under various conditions makes it a preferred choice in the production of complex peptides.
  • Drug Development: The unique structure of this compound can be leveraged in the design of novel pharmaceuticals, particularly in the development of targeted therapies. Its ability to form stable interactions with biological targets enhances its potential in medicinal chemistry.
  • Bioconjugation: It is used in bioconjugation processes, where it can attach to biomolecules like proteins or antibodies. This application is crucial in creating targeted drug delivery systems, improving the efficacy of therapeutic agents.
  • Material Science: The compound can be incorporated into polymer systems, contributing to the development of advanced materials with specific properties, such as increased flexibility or enhanced chemical resistance, suitable for various industrial applications.
  • Research in Organic Chemistry: As a versatile building block, it aids in the synthesis of other complex organic molecules, facilitating research in organic synthesis and helping chemists explore new chemical pathways and reactions.

Citas