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Catalog Number:
20901
CAS Number:
82923-75-9
Acide 1-acétyl-2,3-dihydro-1 H -indole-2-carboxylique
Purity:
≥ 95%
Synonym(s):
Acide N- acétyl-2,3-dihydroindole-2-carboxylique
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$93.14 /100 mg
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Product Information

1-Acetyl-2,3-dihydro-1H-indole-2-carboxylic acid is a versatile compound that has garnered attention in various fields, particularly in medicinal chemistry and organic synthesis. This compound features a unique indole structure, which is known for its biological activity and potential therapeutic applications. Researchers have explored its use in the development of novel pharmaceuticals, particularly in the synthesis of indole-based compounds that exhibit anti-inflammatory and analgesic properties. Its ability to serve as a building block in complex organic reactions makes it invaluable for chemists looking to create diverse molecular architectures.

Moreover, 1-Acetyl-2,3-dihydro-1H-indole-2-carboxylic acid is recognized for its stability and ease of handling, which are critical attributes in both laboratory and industrial settings. Its applications extend to the production of agrochemicals and dyes, where its indole framework contributes to the desired properties of the final products. With its promising potential in drug discovery and material science, this compound is an essential addition to the toolkit of researchers and industry professionals alike.

Synonyms
Acide N- acétyl-2,3-dihydroindole-2-carboxylique
CAS Number
82923-75-9
Purity
≥ 95%
Molecular Formula
C 11 H 11 NON 3
Molecular Weight
205.21
MDL Number
MFCD02258918
PubChem ID
10058771
Melting Point
193-197 ?C
Appearance
Solide marron
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Acide N- acétyl-2,3-dihydroindole-2-carboxylique
CAS Number
82923-75-9
Purity
≥ 95%
Molecular Formula
C 11 H 11 NON 3
Molecular Weight
205.21
MDL Number
MFCD02258918
PubChem ID
10058771
Melting Point
193-197 ?C
Appearance
Solide marron
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

1-Acetyl-2,3-dihydro-1H-indole-2-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders.
  • Biochemical Research: It is used in studies investigating enzyme inhibition and receptor binding, providing insights into cellular mechanisms and potential drug interactions.
  • Material Science: The compound can be incorporated into polymer formulations, enhancing the mechanical properties and thermal stability of materials used in various applications.
  • Natural Product Synthesis: Researchers utilize it in the synthesis of indole derivatives, which are important in creating natural products with medicinal properties.
  • Analytical Chemistry: It is employed as a standard in chromatographic techniques, aiding in the identification and quantification of similar compounds in complex mixtures.

Citations