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Catalog Number:
04979
CAS Number:
204320-59-2
Acide Fmoc-( R , S )-1,3-dihydro-2 H -isoindole carboxylique
Purity:
≥ 97,5 % (HPLC)
Synonym(s):
Disque Fmoc-DL-OH
Documents
$93.14 /250 mg
Taille
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Product Information

Fmoc-(R,S)-1,3-dihydro-2H-isoindole carboxylic acid is a versatile compound widely utilized in the field of 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 allows for efficient coupling reactions, making it an ideal choice for researchers looking to streamline their synthesis processes.

In addition to its role in peptide synthesis, Fmoc-(R,S)-1,3-dihydro-2H-isoindole carboxylic acid has potential applications in drug discovery and development, particularly in the design of bioactive compounds. Its ability to facilitate the formation of complex molecular structures opens avenues for the creation of novel therapeutics. Researchers benefit from its stability and ease of use, which can lead to increased yields and reduced reaction times compared to other similar compounds. This makes it a valuable addition to any laboratory focused on advancing peptide-based research and development.

Synonyms
Disque Fmoc-DL-OH
CAS Number
204320-59-2
Purity
≥ 97,5 % (HPLC)
Molecular Formula
C 24 H 194
Molecular Weight
385.43
MDL Number
MFCD00270204
PubChem ID
2756130
Appearance
Solide blanc
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Disque Fmoc-DL-OH
CAS Number
204320-59-2
Purity
≥ 97,5 % (HPLC)
Molecular Formula
C 24 H 194
Molecular Weight
385.43
MDL Number
MFCD00270204
PubChem ID
2756130
Appearance
Solide blanc
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-(R,S)-1,3-dihydro-2H-isoindole carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure aids in the design of novel pharmaceutical compounds, particularly in the development of drugs targeting neurological disorders.
  • Bioconjugation: The chemical is employed in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Material Science: It is used in the synthesis of advanced materials, such as polymers and nanomaterials, which have applications in electronics and coatings.
  • Research in Organic Chemistry: This compound is a valuable tool for organic chemists studying reaction mechanisms and developing new synthetic methodologies.

Citations