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Catalog Number:
33579
CAS Number:
857478-30-9
Ácido Fmoc-( S )-2-amino-2-metilbutírico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-Isovalina
Documents
$64.90 /100 mg
Tamaño
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Product Information

Fmoc-(S)-2-Amino-2-methylbutyric 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 amino groups during peptide assembly. 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 (S)-configuration enhances its relevance in chiral synthesis, providing an advantage in the production of enantiomerically pure substances, which are crucial in pharmaceutical applications.

In addition to its role in peptide synthesis, Fmoc-(S)-2-Amino-2-methylbutyric acid has been employed in the development of novel therapeutics and bioactive molecules. Its stability and compatibility with various coupling reagents make it a preferred choice for researchers aiming to streamline their synthesis processes. By incorporating this compound into their workflows, scientists can achieve higher yields and purities, ultimately accelerating their research and development timelines.

Synonyms
Fmoc-L-Isovalina
CAS Number
857478-30-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C20H21NO4
Molecular Weight
339.39
MDL Number
MFCD12031688
PubChem ID
73006883
Appearance
Sólido de color blanquecino a blanco grisáceo
Optical Rotation
[a] 20 D = 6 ± 2 ° (C = 1 en DCM) 20 D = 23 ± 2 ° (C = 1 en agua)
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Fmoc-L-Isovalina
CAS Number
857478-30-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C20H21NO4
Molecular Weight
339.39
MDL Number
MFCD12031688
PubChem ID
73006883
Appearance
Sólido de color blanquecino a blanco grisáceo
Optical Rotation
[a] 20 D = 6 ± 2 ° (C = 1 en DCM) 20 D = 23 ± 2 ° (C = 1 en agua)
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(S)-2-Amino-2-methylbutyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound is a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing for the efficient assembly of complex peptide sequences.
  • Drug Development: It plays a crucial role in the pharmaceutical industry, where it is used to develop peptide-based drugs, enhancing the efficacy and specificity of therapeutic agents.
  • Bioconjugation: Researchers use this chemical to facilitate bioconjugation processes, linking peptides to other biomolecules for targeted drug delivery systems, improving treatment outcomes.
  • Research in Neuroscience: It is employed in studies related to neuropeptides, helping scientists understand neurological functions and develop treatments for neurodegenerative diseases.
  • Analytical Chemistry: The compound is utilized in analytical methods to study protein interactions, providing insights into biochemical pathways and potential therapeutic targets.

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