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Catalog Number:
33623
CAS Number:
1217512-55-4
Fmoc-D-octahydroindole-2-carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-D-Oic-OH, (2R,3aS,7aS)-1-Fmoc-octahydro-1H-indole-2-carboxylic acid
Documents
$77.82 /100MG
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Product Information

Fmoc-D-octahydroindole-2-carboxylic acid is a versatile compound widely utilized in the field of peptide synthesis and drug development. This amino acid derivative features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which is crucial for the selective protection of amine functionalities during the synthesis of peptides. Its unique octahydroindole structure enhances its stability and solubility, making it an ideal choice for researchers looking to create complex peptide sequences with high purity and yield.

In practical applications, Fmoc-D-octahydroindole-2-carboxylic acid is particularly valuable in the pharmaceutical industry for the development of bioactive peptides and potential drug candidates. Its ability to facilitate the incorporation of non-standard amino acids into peptide chains allows for the exploration of novel therapeutic agents. Additionally, its compatibility with various coupling reagents and solid-phase synthesis techniques makes it a preferred choice among chemists and researchers. With its robust performance and adaptability, this compound stands out as a key player in advancing peptide chemistry and drug discovery.

Synonyms
Fmoc-D-Oic-OH, (2R,3aS,7aS)-1-Fmoc-octahydro-1H-indole-2-carboxylic acid
CAS Number
1217512-55-4
Purity
≥ 98% (HPLC)
Molecular Formula
C24H25NO4
Molecular Weight
391.46
MDL Number
MFCD12198183
PubChem ID
4712582
Melting Point
169 - 180 ?C
Appearance
White powder
Optical Rotation
[a]D20 = 66 ± 1 ° (C=1 in EtOH)
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Fmoc-D-Oic-OH, (2R,3aS,7aS)-1-Fmoc-octahydro-1H-indole-2-carboxylic acid
CAS Number
1217512-55-4
Purity
≥ 98% (HPLC)
Molecular Formula
C24H25NO4
Molecular Weight
391.46
MDL Number
MFCD12198183
PubChem ID
4712582
Melting Point
169 - 180 ?C
Appearance
White powder
Optical Rotation
[a]D20 = 66 ± 1 ° (C=1 in EtOH)
Conditions
Store at 2 - 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-D-octahydroindole-2-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 structural properties make it a valuable intermediate in the synthesis of bioactive compounds, particularly in the pharmaceutical industry where complex molecules are required.
  • Material Science: The compound can be used in the development of novel polymers and materials, enhancing their mechanical properties and thermal stability.
  • Bioconjugation: Fmoc-D-octahydroindole-2-carboxylic acid is useful in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules for diagnostic and therapeutic applications.
  • Research in Neuroscience: Its derivatives are being explored for their potential effects on neurotransmitter systems, contributing to studies aimed at understanding neurological disorders.

Citations