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Catalog Number:
33708
CAS Number:
501331-02-8
Acide Fmoc-( R )-2-(aminométhyl)-3-méthylbutanoïque
Purity:
≥ 99 % (HPLC)
Documents
$180.00 /25 mg
Taille
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Product Information

(R)-Fmoc-2-aminomethyl-3-methyl-butyric acid is a valuable compound widely utilized in the field of peptide synthesis and drug development. This amino acid derivative, characterized by its fluorenylmethoxycarbonyl (Fmoc) protecting group, offers enhanced stability and solubility, making it an ideal choice for researchers working on complex peptide sequences. Its unique structure allows for efficient coupling reactions, facilitating the synthesis of peptides with high purity and yield. This compound is particularly beneficial in the pharmaceutical industry, where it plays a crucial role in the development of therapeutic peptides and biologics.

In addition to its applications in peptide synthesis, (R)-Fmoc-2-aminomethyl-3-methyl-butyric acid is also recognized for its potential in various research areas, including medicinal chemistry and biochemistry. Its ability to serve as a building block for more complex molecules opens up possibilities for innovative drug design and development. Researchers appreciate its compatibility with standard coupling reagents and its effectiveness in solid-phase peptide synthesis, making it a preferred choice for both academic and industrial applications.

CAS Number
501331-02-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 21 H 234
Molecular Weight
353.41
MDL Number
MFCD07372882
PubChem ID
53397703
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -21 ± 2 º (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
CAS Number
501331-02-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 21 H 234
Molecular Weight
353.41
MDL Number
MFCD07372882
PubChem ID
53397703
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -21 ± 2 º (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(R)-Fmoc-2-aminomethyl-3-methyl-butyric acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without interfering with other functional groups. This is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: It plays a significant role in the design of drug candidates, particularly in creating compounds that can effectively target specific biological pathways, enhancing the efficacy of new medications.
  • Bioconjugation: The compound is used to attach biomolecules to surfaces or other molecules, which is essential in creating targeted therapies and diagnostic tools in the biomedical field.
  • Research in Neuroscience: It aids in the synthesis of neuropeptides, which are vital for understanding neurological processes and developing treatments for neurological disorders.
  • Custom Chemical Synthesis: This compound is favored in custom synthesis projects due to its versatility and ability to enhance the stability and solubility of various chemical entities, making it a valuable tool for researchers.

Citations