Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
02717
CAS Number:
109523-13-9
Boc-L-octahydroindole-2-carboxylic acid
Purity:
≥ 97% (HPLC)
Synonym(s):
Boc-L-Oic-OH, (2S,3aS,7aS)-1-Boc-octahydro-1H-indole-2-carboxylic acid
Documents
$51.18 /250MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Boc-L-octahydroindole-2-carboxylic acid is a versatile compound widely utilized in the synthesis of peptides and pharmaceuticals. This amino acid derivative features a unique bicyclic structure that enhances its stability and solubility, making it an ideal choice for researchers and industry professionals engaged in drug development and peptide synthesis. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective reactions, facilitating the incorporation of this compound into complex molecular architectures.

In the pharmaceutical industry, Boc-L-octahydroindole-2-carboxylic acid serves as a valuable building block for the development of bioactive compounds, particularly in the creation of novel therapeutics targeting various diseases. Its unique properties enable the formation of diverse peptide sequences, which can lead to the discovery of new drug candidates. Additionally, its application in medicinal chemistry and biochemistry underscores its importance in advancing research and innovation in drug design.

Synonyms
Boc-L-Oic-OH, (2S,3aS,7aS)-1-Boc-octahydro-1H-indole-2-carboxylic acid
CAS Number
109523-13-9
Purity
≥ 97% (HPLC)
Molecular Formula
C14H23NO4
Molecular Weight
269.3
MDL Number
MFCD09750486
PubChem ID
4712510
Melting Point
131-137 ?C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -24 ± 3 º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-Oic-OH, (2S,3aS,7aS)-1-Boc-octahydro-1H-indole-2-carboxylic acid
CAS Number
109523-13-9
Purity
≥ 97% (HPLC)
Molecular Formula
C14H23NO4
Molecular Weight
269.3
MDL Number
MFCD09750486
PubChem ID
4712510
Melting Point
131-137 ?C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -24 ± 3 º (C=1 in MeOH)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of cyclic peptides that have unique biological activities.
  • Drug Development: It is used in the pharmaceutical industry for the creation of novel drug candidates, especially those targeting neurological disorders, due to its structural properties that mimic neurotransmitters.
  • Bioconjugation: The compound can be employed in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other compounds, enhancing drug delivery systems.
  • Research in Organic Chemistry: It is a key intermediate in various organic synthesis reactions, helping chemists explore new synthetic pathways and improve reaction efficiencies.
  • Material Science: The compound finds applications in the development of new materials, particularly in creating polymers with specific properties for use in coatings or adhesives.

Citations