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Catalog Number:
21537
CAS Number:
22948-94-3
N-Acetylindole-3-carboxaldehyde
Purity:
≥ 99% (HPLC)
Synonym(s):
1-Acetyl-1H-indole-3-carbaldehyde, N-Acetylindole-3-aldehyde
Documents
$117.78 /25G
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Product Information

N-Acetylindole-3-carboxaldehyde is a versatile compound with significant applications in the fields of organic synthesis and medicinal chemistry. This compound, also known as 1-acetylindole-3-carbaldehyde, features a unique structure that allows it to serve as an important intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its reactivity and functional groups make it particularly useful in the development of indole-based compounds, which are known for their diverse biological activities, including anti-inflammatory and anticancer properties. Researchers have utilized N-Acetylindole-3-carboxaldehyde in the synthesis of novel drug candidates, showcasing its potential to contribute to advancements in therapeutic agents.

In addition to its synthetic utility, N-Acetylindole-3-carboxaldehyde is recognized for its role in the development of fluorescent probes and materials science applications. Its ability to form stable derivatives enhances its relevance in the design of sensors and imaging agents. The compound's unique properties, combined with its ease of use in laboratory settings, make it an attractive choice for researchers looking to explore new avenues in chemical research and development.

Synonyms
1-Acetyl-1H-indole-3-carbaldehyde, N-Acetylindole-3-aldehyde
CAS Number
22948-94-3
Purity
≥ 99% (HPLC)
Molecular Formula
C11H9NO2
Molecular Weight
187.2
MDL Number
MFCD00039691
PubChem ID
89915
Melting Point
161-168 °C
Appearance
Yellowish crystal
Conditions
Store at 0-8 °C
General Information
Synonyms
1-Acetyl-1H-indole-3-carbaldehyde, N-Acetylindole-3-aldehyde
CAS Number
22948-94-3
Purity
≥ 99% (HPLC)
Molecular Formula
C11H9NO2
Molecular Weight
187.2
MDL Number
MFCD00039691
PubChem ID
89915
Melting Point
161-168 °C
Appearance
Yellowish crystal
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

N-Acetylindole-3-carboxaldehyde is widely utilized in research focused on

  • Synthesis of Pharmaceuticals: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.
  • Fluorescent Probes: It is used in the development of fluorescent probes for biological imaging, allowing researchers to visualize cellular processes in real-time, which is crucial for drug discovery and development.
  • Organic Synthesis: N-Acetylindole-3-carboxaldehyde is a valuable building block in organic synthesis, facilitating the creation of complex organic molecules with applications in materials science and nanotechnology.
  • Research in Biochemistry: The compound is employed in biochemical studies to explore enzyme interactions and metabolic pathways, providing insights into cellular functions and disease mechanisms.
  • Development of Agrochemicals: It plays a role in the formulation of agrochemicals, contributing to the design of more effective pesticides and herbicides that are safer for the environment.

Citations