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

Catalog Number:
29033
CAS Number:
1018899-99-4
Ácido Fmoc-( R -2-(aminometil)-4-metilpentanoico
Purity:
≥ 99 % (HPLC)
Synonym(s):
(Ácido R -Fmoc-2-aminometil-4-metil-pentanoico, ( R -Fmoc-β2-homoleucina
Documents
$234.85 /25 mg
Tamaño
Request Bulk Quote
Product Information

Fmoc-(R)-2-(aminomethyl)-4-methylpentanoic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure allows for efficient coupling reactions, making it an ideal choice for researchers focused on developing complex peptides and biologically active compounds. The (R)-configuration enhances its applicability in chiral synthesis, providing an edge in producing enantiomerically pure products that are crucial in pharmaceutical applications.

In addition to its role in peptide synthesis, Fmoc-(R)-2-(aminomethyl)-4-methylpentanoic acid is also valuable in the development of novel therapeutic agents and biomaterials. Its stability under various reaction conditions and compatibility with a range of coupling reagents make it a preferred choice for chemists looking to streamline their synthesis processes. Whether in academic research or industrial applications, this compound offers significant advantages in efficiency and product quality, making it an essential tool for professionals in the field.

Synonyms
(Ácido R -Fmoc-2-aminometil-4-metil-pentanoico, ( R -Fmoc-β2-homoleucina
CAS Number
1018899-99-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H25NO4
Molecular Weight
367.44
MDL Number
MFCD07372889
PubChem ID
53397704
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -11 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
(Ácido R -Fmoc-2-aminometil-4-metil-pentanoico, ( R -Fmoc-β2-homoleucina
CAS Number
1018899-99-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H25NO4
Molecular Weight
367.44
MDL Number
MFCD07372889
PubChem ID
53397704
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -11 ± 2º (C=1 en DMF)
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

Fmoc-(R)-2-(aminomethyl)-4-methylpentanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its application in the synthesis of peptide-based drugs is significant, as it helps in creating more stable and effective therapeutic agents.
  • Bioconjugation: The compound is used in bioconjugation processes to attach peptides to various biomolecules, enhancing the specificity and efficacy of targeted therapies.
  • Research in Neuroscience: It plays a role in the development of neuropeptides, which are crucial for understanding neurological functions and disorders.
  • Custom Synthesis Services: Many laboratories utilize this compound for custom synthesis projects, providing tailored solutions for specific research needs in the pharmaceutical and biotechnology sectors.

Citas