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Catalog Number:
33622
Ácido Boc-D-octahidroindol-2-carboxílico
Synonym(s):
Boc-D-Oic-OH, ( 2R , 3aS , 7aS -1-Boc-octahidro- 1H -indol-2-ácido carboxílico
Documents
$79.22 /100 mg
Tamaño
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Product Information

Boc-D-octahydroindole-2-carboxylic acid is a versatile compound widely utilized in the field of organic synthesis and pharmaceutical research. This compound, known for its unique bicyclic structure, serves as a valuable building block in the development of various bioactive molecules. Its protective Boc (tert-butyloxycarbonyl) group enhances its stability and solubility, making it an ideal candidate for peptide synthesis and other complex organic reactions. Researchers appreciate its role in the synthesis of indole derivatives, which are crucial in the design of pharmaceuticals targeting a range of therapeutic areas, including oncology and neurology.

In addition to its applications in drug development, Boc-D-octahydroindole-2-carboxylic acid is also explored for its potential in materials science and catalysis. Its unique structural properties enable the creation of novel materials with specific functionalities, making it a compound of interest for researchers aiming to innovate in polymer chemistry and nanotechnology. With its broad applicability and significant advantages over similar compounds, Boc-D-octahydroindole-2-carboxylic acid stands out as a key ingredient for advancing research and development in multiple scientific domains.

Synonyms
Boc-D-Oic-OH, ( 2R , 3aS , 7aS -1-Boc-octahidro- 1H -indol-2-ácido carboxílico
Molecular Formula
C14H23NO4
Molecular Weight
269.34
MDL Number
MFCD12198182
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Boc-D-Oic-OH, ( 2R , 3aS , 7aS -1-Boc-octahidro- 1H -indol-2-ácido carboxílico
Molecular Formula
C14H23NO4
Molecular Weight
269.34
MDL Number
MFCD12198182
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-D-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 without unwanted side reactions. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: In pharmaceutical research, it can be used to develop new drug candidates, particularly in creating compounds that target specific biological pathways, enhancing efficacy and reducing side effects.
  • Material Science: The compound can be incorporated into polymers to create materials with unique properties, such as increased flexibility or improved thermal stability, which are valuable in various industrial applications.
  • Biological Research: It is useful in studying biological processes due to its ability to mimic natural compounds, aiding researchers in understanding complex biochemical pathways and interactions.
  • Analytical Chemistry: This chemical can be utilized in the development of analytical methods for detecting and quantifying other compounds, providing a reliable tool for quality control in laboratories.

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