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Catalog Number:
22748
CAS Number:
166881-43-2
Fmoc- N -(2,4,6-triméthoxybenzyl)-glycine
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-TmbGly-OH
Documents
$154.93 /250 mg
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Product Information

Fmoc-N-(2,4,6-trimethoxybenzyl)-glycine 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 amines during the synthesis of peptides. Its unique structure, characterized by the presence of a 2,4,6-trimethoxybenzyl moiety, enhances its stability and solubility, making it an ideal choice for researchers focused on developing complex peptide sequences.

This compound is particularly valuable in the pharmaceutical industry for the synthesis of bioactive peptides, which can serve as potential therapeutics in various medical applications. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups allows for the efficient production of peptides with high purity. Researchers can leverage Fmoc-N-(2,4,6-trimethoxybenzyl)-glycine to streamline their workflows, reduce synthesis times, and improve yields, ultimately advancing their projects in drug discovery and development.

Synonyms
Fmoc-TmbGly-OH
CAS Number
166881-43-2
Purity
≥ 97 % (HPLC)
Molecular Formula
C 27 H 277
Molecular Weight
477.51
MDL Number
MFCD09952622
PubChem ID
56777269
Melting Point
148-155 °C
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-TmbGly-OH
CAS Number
166881-43-2
Purity
≥ 97 % (HPLC)
Molecular Formula
C 27 H 277
Molecular Weight
477.51
MDL Number
MFCD09952622
PubChem ID
56777269
Melting Point
148-155 °C
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-N-(2,4,6-trimethoxybenzyl)-glycine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex molecules for drug development and biological studies.
  • Drug Discovery: Its unique structure enhances the ability to design and test new pharmaceuticals, particularly in the fields of oncology and neurology, where targeted therapies are crucial.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules to therapeutic agents, which is essential in developing targeted drug delivery systems.
  • Research in Neuroscience: It plays a role in the study of neuropeptides, helping scientists understand brain function and develop treatments for neurological disorders.
  • Analytical Chemistry: This chemical is useful in analytical techniques, such as HPLC, for separating and analyzing complex mixtures, which is vital for quality control in pharmaceuticals.

Citations