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Catalog Number:
21621
CAS Number:
244-63-3
9H-Pyrido[3,4-b]indole
Purity:
≥ 98% (Assay)
Synonym(s):
2,9-Diazafluorene, Norharmane
Documents
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Product Information

9H-Pyrido[3,4-b]indole is a versatile heterocyclic compound that has garnered attention in various fields, particularly in medicinal chemistry and organic synthesis. This compound is recognized for its unique structural features, which contribute to its potential as a building block in the development of pharmaceuticals and agrochemicals. Its ability to act as a scaffold for diverse chemical modifications makes it a valuable asset in drug discovery, especially in the synthesis of bioactive molecules that target various biological pathways.

Researchers have explored the applications of 9H-Pyrido[3,4-b]indole in the development of novel therapeutic agents, particularly in the treatment of cancer and neurological disorders. Its distinct electronic properties and ability to interact with biological systems enhance its utility in creating compounds with improved efficacy and selectivity. Additionally, its stability and compatibility with various reaction conditions make it an ideal candidate for use in complex organic syntheses. As such, 9H-Pyrido[3,4-b]indole stands out as a promising compound for professionals seeking innovative solutions in drug development and chemical research.

Synonyms
2,9-Diazafluorene, Norharmane
CAS Number
244-63-3
Purity
≥ 98% (Assay)
Molecular Formula
C11H8N2
Molecular Weight
168.2
MDL Number
MFCD00004956
PubChem ID
64961
Melting Point
196 - 204 °C
Appearance
White to off-white or yellow powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
2,9-Diazafluorene, Norharmane
CAS Number
244-63-3
Purity
≥ 98% (Assay)
Molecular Formula
C11H8N2
Molecular Weight
168.2
MDL Number
MFCD00004956
PubChem ID
64961
Melting Point
196 - 204 °C
Appearance
White to off-white or yellow powder
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

9H-Pyrido[3,4-b]indole is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a scaffold for designing new drugs, particularly in the development of anti-cancer agents due to its ability to inhibit specific cancer cell lines.
  • Neuroscience Research: It is used in studies investigating neuroprotective effects, potentially aiding in the treatment of neurodegenerative diseases like Alzheimer's and Parkinson's.
  • Material Science: The compound is explored for its properties in creating advanced materials, such as organic semiconductors, which are essential for developing efficient electronic devices.
  • Biological Activity Studies: Researchers utilize it to examine various biological activities, including antimicrobial and anti-inflammatory effects, which can lead to new therapeutic options.
  • Natural Product Synthesis: It is often a key intermediate in the synthesis of complex natural products, facilitating the discovery of new compounds with beneficial properties.

Citations