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Catalog Number:
35206
CAS Number:
288617-75-4
Acide Fmoc-( S -2-amino-2-méthyl-déc-6-énoïque
Purity:
≥ 98 % (HPLC chirale, HPLC)
Synonym(s):
Fmoc-( S -2-(7-octényl)Ala-OH, Fmoc-α-Me-Gly(octényl)-OH
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$192.19 /250 mg
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Product Information

Fmoc-(S)-2-amino-2-methyl-dec-6-enoic 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 not only enhances stability but also facilitates the introduction of complex functionalities, making it an ideal choice for researchers focused on developing novel therapeutic agents.

In the pharmaceutical industry, Fmoc-(S)-2-amino-2-methyl-dec-6-enoic acid serves as a crucial intermediate in the synthesis of bioactive peptides and proteins. Its application extends to the development of targeted drug delivery systems and the design of peptide-based vaccines. The compound’s ability to undergo various coupling reactions while maintaining high purity levels makes it a preferred choice for chemists and researchers aiming for efficiency and reliability in their synthetic processes.

Synonyms
Fmoc-( S -2-(7-octényl)Ala-OH, Fmoc-α-Me-Gly(octényl)-OH
CAS Number
288617-75-4
Purity
≥ 98 % (HPLC chirale, HPLC)
Molecular Formula
C 26 H 314
Molecular Weight
421.53
MDL Number
MFCD12925760
PubChem ID
53395081
Appearance
Semi-solide blanc cassé
Optical Rotation
[a] D 20 = 9 ± 1 ° (C = 1 dans EtOH)
Conditions
Magasin chez RT
General Information
Synonyms
Fmoc-( S -2-(7-octényl)Ala-OH, Fmoc-α-Me-Gly(octényl)-OH
CAS Number
288617-75-4
Purity
≥ 98 % (HPLC chirale, HPLC)
Molecular Formula
C 26 H 314
Molecular Weight
421.53
MDL Number
MFCD12925760
PubChem ID
53395081
Appearance
Semi-solide blanc cassé
Optical Rotation
[a] D 20 = 9 ± 1 ° (C = 1 dans EtOH)
Conditions
Magasin chez RT
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-amino-2-methyl-dec-6-enoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex and diverse peptide sequences.
  • Drug Development: Its unique structure can be employed in the design of novel pharmaceuticals, especially in targeting specific biological pathways, enhancing drug efficacy and specificity.
  • Bioconjugation: The chemical is useful in bioconjugation processes, where it can be attached to biomolecules for the development of targeted therapies, improving the delivery of drugs to specific cells.
  • Research in Neuroscience: It can be utilized in the study of neuropeptides, contributing to research aimed at understanding neurological functions and disorders, potentially leading to new treatment options.
  • Material Science: This compound can be incorporated into polymers for creating advanced materials with specific properties, such as enhanced biocompatibility for medical devices.

Citations