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Catalog Number:
21274
CAS Number:
10553-14-7
7-nitroindole-3-carboxaldéhyde
Purity:
≥ 95 % (HPLC)
Synonym(s):
7-Nitro-1H-indole-3-carbaldéhyde
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Product Information

7-Nitroindole-3-carboxaldehyde is a versatile compound widely recognized for its applications in organic synthesis and pharmaceutical research. This compound, characterized by its nitro and aldehyde functional groups, serves as a valuable intermediate in the synthesis of various biologically active molecules. Researchers utilize 7-Nitroindole-3-carboxaldehyde in the development of novel pharmaceuticals, particularly in the creation of indole-based compounds that exhibit significant biological activity, including anti-inflammatory and anticancer properties. Its unique structure allows for easy modification, making it an ideal candidate for medicinal chemistry applications.

In addition to its role in drug discovery, 7-Nitroindole-3-carboxaldehyde is also employed in the synthesis of fluorescent probes and dyes, enhancing its utility in biochemical research. The compound's ability to participate in diverse chemical reactions, such as condensation and coupling reactions, further underscores its importance in synthetic organic chemistry. With its broad range of applications, 7-Nitroindole-3-carboxaldehyde stands out as a crucial building block for researchers and industry professionals aiming to innovate in the fields of pharmaceuticals and materials science.

Synonyms
7-Nitro-1H-indole-3-carbaldéhyde
CAS Number
10553-14-7
Purity
≥ 95 % (HPLC)
Molecular Formula
C9H6N2O3
Molecular Weight
190.16
MDL Number
MFCD01074519
PubChem ID
2762438
Appearance
Vert clair solide
Conditions
Conserver à 0-8°C
General Information
Synonyms
7-Nitro-1H-indole-3-carbaldéhyde
CAS Number
10553-14-7
Purity
≥ 95 % (HPLC)
Molecular Formula
C9H6N2O3
Molecular Weight
190.16
MDL Number
MFCD01074519
PubChem ID
2762438
Appearance
Vert clair solide
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

7-Nitroindole-3-carboxaldehyde is widely utilized in research focused on:

  • Synthetic Organic Chemistry: This compound serves as a building block for synthesizing various nitrogen-containing heterocycles, which are crucial in developing pharmaceuticals and agrochemicals.
  • Fluorescent Probes: Its unique properties make it suitable for creating fluorescent probes used in biological imaging, helping researchers visualize cellular processes in real-time.
  • Drug Development: The compound is explored for its potential therapeutic effects, particularly in neuropharmacology, where it may influence neurotransmitter systems.
  • Material Science: It is used in the formulation of advanced materials, such as polymers and coatings, that require specific optical or electronic properties.
  • Biochemical Research: This chemical acts as a reagent in various biochemical assays, aiding in the study of enzyme activities and molecular interactions.

Citations