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Catalog Number:
02718
CAS Number:
130309-37-4
Fmoc-L-octahydroindole-2-carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Oic-OH, (2S,3aS,7aS)-1-Fmoc-octahydro-1H-indole-2-carboxylic acid
Documents
$25.00 /250MG
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Product Information

Fmoc-L-octahydroindole-2-carboxylic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a unique octahydroindole structure, which enhances its utility in the design of bioactive peptides and pharmaceuticals. The Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for selective deprotection during synthesis, making it an ideal choice for researchers focused on complex peptide sequences. Its application extends to the development of novel therapeutic agents, particularly in the fields of oncology and neurology, where such compounds can mimic natural biological processes.

Researchers appreciate Fmoc-L-octahydroindole-2-carboxylic acid for its stability and ease of use in various organic reactions. Its ability to facilitate the synthesis of cyclic peptides and other complex structures positions it as a valuable tool in medicinal chemistry. With its favorable properties, this compound not only streamlines the synthesis process but also enhances the overall yield and purity of the final products, making it a preferred choice among professionals in the pharmaceutical industry.

Synonyms
Fmoc-L-Oic-OH, (2S,3aS,7aS)-1-Fmoc-octahydro-1H-indole-2-carboxylic acid
CAS Number
130309-37-4
Purity
≥ 98% (HPLC)
Molecular Formula
C24H25NO4
Molecular Weight
391.5
MDL Number
MFCD09750487
PubChem ID
4712582
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -25 ± 3º (C=1 in DMF) [a]D20 = -38 ± 3º (C=1 in EtOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-Oic-OH, (2S,3aS,7aS)-1-Fmoc-octahydro-1H-indole-2-carboxylic acid
CAS Number
130309-37-4
Purity
≥ 98% (HPLC)
Molecular Formula
C24H25NO4
Molecular Weight
391.5
MDL Number
MFCD09750487
PubChem ID
4712582
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -25 ± 3º (C=1 in DMF) [a]D20 = -38 ± 3º (C=1 in EtOH)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-L-octahydroindole-2-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions and improving yield and purity.
  • Drug Development: Its structural properties make it valuable in the design of novel pharmaceuticals, particularly in the development of compounds targeting neurological conditions.
  • Bioconjugation: The chemical is employed in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Material Science: It is used in the creation of advanced materials, particularly in the development of polymers with specific functionalities for applications in coatings and adhesives.
  • Research in Organic Chemistry: The compound is a key reagent in various organic synthesis pathways, providing researchers with a versatile tool for exploring new chemical reactions.

Citations