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Catalog Number:
21016
CAS Number:
169789-47-3
5-Etoxi- 1H- indol-3-carbaldehído
Purity:
≥ 95 % (HPLC)
Synonym(s):
5-Etoxi-3-indolcarboxaldehído, 5-Etoxiindol-3-aldehído
Documents
$120.88 /250 mg
Tamaño
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Product Information

5-Ethoxy-1H-indole-3-carbaldehyde is a versatile compound recognized for its significant applications in organic synthesis and medicinal chemistry. This compound features a unique indole structure, which is pivotal in the development of various pharmaceuticals and agrochemicals. Its ethoxy group enhances its solubility and reactivity, making it an ideal candidate for synthesizing more complex molecules. Researchers have utilized 5-Ethoxy-1H-indole-3-carbaldehyde in the synthesis of indole derivatives, which are known for their diverse biological activities, including anti-inflammatory and anticancer properties.

In addition to its role in drug discovery, this compound serves as a valuable intermediate in the production of dyes and pigments, further broadening its industrial relevance. Its unique properties allow for modifications that can lead to the development of novel compounds with enhanced efficacy. The compound's ability to facilitate complex reactions while maintaining stability makes it a preferred choice among professionals in both research and industrial settings.

Synonyms
5-Etoxi-3-indolcarboxaldehído, 5-Etoxiindol-3-aldehído
CAS Number
169789-47-3
Purity
≥ 95 % (HPLC)
Molecular Formula
C11H11NO2
Molecular Weight
189.21
MDL Number
MFCD07364715
PubChem ID
4777881
Appearance
Sólido de color amarillo a marrón pálido.
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
5-Etoxi-3-indolcarboxaldehído, 5-Etoxiindol-3-aldehído
CAS Number
169789-47-3
Purity
≥ 95 % (HPLC)
Molecular Formula
C11H11NO2
Molecular Weight
189.21
MDL Number
MFCD07364715
PubChem ID
4777881
Appearance
Sólido de color amarillo a marrón pálido.
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-Ethoxy-1H-indole-3-carbaldehyde 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, enhancing drug development efficiency.
  • Fluorescent Probes: It is used in the creation of fluorescent probes for biological imaging, allowing researchers to visualize cellular processes with high specificity and sensitivity.
  • Organic Electronics: The compound finds application in organic electronics, particularly in the development of organic light-emitting diodes (OLEDs), contributing to advancements in display technologies.
  • Material Science: It plays a role in the formulation of advanced materials, such as polymers and coatings, which exhibit improved thermal and mechanical properties.
  • Biochemical Research: This chemical is valuable in biochemical research for studying enzyme activity and protein interactions, aiding in the understanding of complex biological systems.

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