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Catalog Number:
21273
CAS Number:
92855-64-6
6-Benzyloxyindole-3-carboxaldéhyde
Purity:
≥ 95 % (HPLC)
Synonym(s):
6-(benzyloxy)-1H-indole-3-carbaldéhyde
Documents
$60.39 /250 mg
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Product Information

6-Benzyloxyindole-3-carboxaldehyde is a versatile compound recognized for its unique structural features and potential applications in various fields, particularly in medicinal chemistry and organic synthesis. This compound, with its phenylmethoxy group, serves as a valuable intermediate in the synthesis of biologically active molecules, including pharmaceuticals and agrochemicals. Its aldehyde functional group enhances its reactivity, making it an excellent candidate for further chemical modifications, which can lead to the development of novel therapeutic agents.

In research settings, 6-Benzyloxyindole-3-carboxaldehyde has been utilized in the synthesis of indole derivatives, which are known for their diverse biological activities, including anti-inflammatory and anticancer properties. The compound's ability to facilitate complex reactions while maintaining stability under various conditions makes it an attractive option for researchers looking to explore new chemical pathways. Its applications extend to the development of fluorescent probes and materials in the field of organic electronics, showcasing its multifaceted utility in both academic and industrial research.

Synonyms
6-(benzyloxy)-1H-indole-3-carbaldéhyde
CAS Number
92855-64-6
Purity
≥ 95 % (HPLC)
Molecular Formula
C 16 H 13 NO 2
Molecular Weight
251.28
MDL Number
MFCD00056931
PubChem ID
22014791
Appearance
Brun clair uni
Conditions
Conserver à 0-8°C
General Information
Synonyms
6-(benzyloxy)-1H-indole-3-carbaldéhyde
CAS Number
92855-64-6
Purity
≥ 95 % (HPLC)
Molecular Formula
C 16 H 13 NO 2
Molecular Weight
251.28
MDL Number
MFCD00056931
PubChem ID
22014791
Appearance
Brun clair uni
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

6-Benzyloxyindole-3-carboxaldehyde is widely utilized in research focused on:

  • Synthesis of Indole Derivatives: This compound serves as a key intermediate in the synthesis of various indole derivatives, which are important in pharmaceuticals and agrochemicals.
  • Drug Development: Its unique structure makes it a valuable candidate for developing new drugs, particularly in the treatment of cancer and neurological disorders.
  • Fluorescent Probes: The compound can be used to create fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes.
  • Organic Electronics: It has potential applications in organic electronics, such as organic light-emitting diodes (OLEDs), due to its electronic properties.
  • Research in Material Science: The compound's properties can be explored in material science for developing novel materials with specific functionalities.

Citations