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Catalog Number:
21999
CAS Number:
1196-70-9
Indole-6-carboxaldéhyde
Purity:
≥ 98 % (HPLC)
Synonym(s):
1 H -Indole-6-carbaldéhyde, 6-Formylindole
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Product Information

Indole-6-carboxaldehyde is a versatile compound recognized for its significant role in organic synthesis and medicinal chemistry. This aromatic aldehyde features a unique indole structure, making it an essential building block in the development of various pharmaceuticals and agrochemicals. Its reactivity allows for the formation of diverse derivatives, which can be utilized in the synthesis of biologically active compounds, including potential anti-cancer agents and anti-inflammatory drugs. Researchers appreciate its ability to facilitate complex reactions, such as the synthesis of heterocyclic compounds, which are crucial in drug discovery and development.

In addition to its applications in pharmaceuticals, Indole-6-carboxaldehyde is also employed in the production of dyes and pigments, enhancing the color properties of various materials. Its unique chemical properties enable it to act as a key intermediate in the synthesis of novel materials with tailored functionalities. With its broad range of applications and the potential for innovation in various fields, Indole-6-carboxaldehyde stands out as a valuable compound for researchers and industry professionals alike.

Synonyms
1 H -Indole-6-carbaldéhyde, 6-Formylindole
CAS Number
1196-70-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 9 H 7 NON
Molecular Weight
145.16
MDL Number
MFCD02179596
PubChem ID
2773435
Melting Point
124-132º C
Appearance
Poudre cristalline brun orangé
Conditions
Conserver à 0-8°C
Safety & Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
General Information
Synonyms
1 H -Indole-6-carbaldéhyde, 6-Formylindole
CAS Number
1196-70-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 9 H 7 NON
Molecular Weight
145.16
MDL Number
MFCD02179596
PubChem ID
2773435
Melting Point
124-132º C
Appearance
Poudre cristalline brun orangé
Conditions
Conserver à 0-8°C
Safety & Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Properties
Additional property information coming soon!
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Applications

Indole-6-carboxaldehyde is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders, due to its ability to interact with specific biological pathways.
  • Fluorescent Probes: It is employed in the development of fluorescent probes for biological imaging, allowing researchers to visualize cellular processes with high specificity and sensitivity.
  • Organic Electronics: Indole-6-carboxaldehyde is used in the fabrication of organic light-emitting diodes (OLEDs), contributing to the advancement of energy-efficient display technologies.
  • Research in Natural Products: The compound is investigated for its role in the synthesis of natural products, enhancing the understanding of complex biochemical pathways and leading to potential new drug discoveries.
  • Biochemical Assays: It is utilized in various biochemical assays to study enzyme activity and metabolic processes, providing valuable insights for both academic and industrial research.

Citations