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

Catalog Number:
29662
CAS Number:
1018332-23-4
Ácido 2R , 4S -Fmoc-4-amino-1-Boc-pirrolidin-2-carboxílico
Purity:
≥ 98 % (HPLC)
Documents
$93.14 /100 mg
Tamaño
Request Bulk Quote
Product Information

The compound (2R,4S)-Fmoc-4-amino-1-Boc-pyrrolidine-2-carboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during peptide assembly. Its Boc (tert-butyloxycarbonyl) group further enhances its utility by providing a stable and easily removable protection for the amino group, making it ideal for complex peptide synthesis. Researchers and industry professionals appreciate its role in developing bioactive peptides, pharmaceuticals, and other biologically relevant compounds.

With its unique structural properties, this compound facilitates the formation of diverse peptide sequences, enabling the exploration of new therapeutic avenues. Its high stability and compatibility with various coupling reagents make it a preferred choice for chemists engaged in peptide research and development. The compound's ability to streamline synthesis processes while maintaining high purity levels positions it as a valuable asset in both academic and industrial laboratories.

CAS Number
1018332-23-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C25H28N2O6
Molecular Weight
452.51
MDL Number
MFCD11519438
PubChem ID
3671690
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = +13 ± 2º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
1018332-23-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C25H28N2O6
Molecular Weight
452.51
MDL Number
MFCD11519438
PubChem ID
3671690
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = +13 ± 2º (C=1 en MeOH)
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

(2R,4S)-Fmoc-4-amino-1-Boc-pyrrolidine-2-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides. Its protective groups allow for selective reactions, making it easier to assemble complex peptide structures.
  • Drug Development: In pharmaceutical research, it is used to create novel drug candidates, particularly in the development of therapeutics targeting various diseases. Its unique structure can enhance bioavailability and efficacy.
  • Bioconjugation: The compound is valuable in bioconjugation processes, where it can be attached to biomolecules for targeted drug delivery systems, improving the specificity and effectiveness of treatments.
  • Research in Neuroscience: It is utilized in studies related to neuroactive compounds, aiding in the development of molecules that can interact with neurotransmitter systems, potentially leading to breakthroughs in treating neurological disorders.
  • Material Science: This chemical is also explored in the development of advanced materials, particularly in creating polymers with specific properties that can be used in various industrial applications.

Citas