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Catalog Number:
29032
CAS Number:
193887-45-5
Acide Fmoc-( S -2-(aminométhyl)-4-méthylpentanoïque
Purity:
≥ 99 % (HPLC)
Synonym(s):
( Acide S -Fmoc-2-aminométhyl-4-méthyl-pentanoïque, ( S -Fmoc-β2-homoleucine
Documents
$234.85 /25 mg
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Product Information

Fmoc-(S)-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 amines during the synthesis of peptides. Its unique structure allows for efficient coupling reactions, making it an ideal choice for researchers focused on developing complex peptide sequences. The compound's chiral center enhances its relevance in the synthesis of enantiomerically pure compounds, which is crucial in pharmaceutical applications where stereochemistry plays a significant role in biological activity.

In addition to its application in peptide synthesis, Fmoc-(S)-2-(aminomethyl)-4-methylpentanoic acid can be employed in the development of novel therapeutics and biomaterials. Its ability to facilitate the formation of peptide bonds while maintaining stability under various reaction conditions makes it a preferred choice for chemists and researchers. This compound not only streamlines the synthesis process but also enhances the overall yield and purity of the final products, making it a valuable asset in both academic and industrial laboratories.

Synonyms
( Acide S -Fmoc-2-aminométhyl-4-méthyl-pentanoïque, ( S -Fmoc-β2-homoleucine
CAS Number
193887-45-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C 22 H 254
Molecular Weight
367.44
MDL Number
MFCD07372888
PubChem ID
53397704
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = +10 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
( Acide S -Fmoc-2-aminométhyl-4-méthyl-pentanoïque, ( S -Fmoc-β2-homoleucine
CAS Number
193887-45-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C 22 H 254
Molecular Weight
367.44
MDL Number
MFCD07372888
PubChem ID
53397704
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = +10 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(S)-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 pharmaceuticals enables researchers to create targeted therapies with improved efficacy and reduced side effects.
  • Bioconjugation: The compound is used in bioconjugation processes, facilitating the attachment of peptides to various biomolecules, which is crucial in developing diagnostic tools and therapeutics.
  • Research in Neuroscience: It plays a role in synthesizing neuropeptides, aiding studies on neurological functions and potential treatments for neurodegenerative diseases.
  • Custom Peptide Libraries: This chemical is instrumental in generating diverse peptide libraries for screening in drug discovery, allowing researchers to identify novel compounds with desired biological activities.

Citations