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Catalog Number:
21543
CAS Number:
6953-22-6
5-benciloxiindol-3-carboxaldehído
Purity:
≥ 98 % (HPLC)
Synonym(s):
5-(benciloxi)-1 H -indol-3-carbaldehído, 5-Benciloxi-3-formilindol
Documents
$22.03 /5G
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Product Information

5-Benzyloxyindole-3-carboxaldehyde is a versatile compound recognized for its significant role in organic synthesis and medicinal chemistry. This compound, also known as 5-phenylmethoxy-1H-indole-3-carbaldehyde, features a unique structure that allows it to serve as an important intermediate in the synthesis of various bioactive molecules. Its ability to undergo further transformations makes it valuable in the development of pharmaceuticals, particularly in the creation of indole-based compounds that exhibit a range of biological activities, including anti-cancer and anti-inflammatory properties.

Researchers and industry professionals appreciate 5-Benzyloxyindole-3-carboxaldehyde for its stability and reactivity, which facilitate the design of complex molecular architectures. Its applications extend to the fields of agrochemicals and materials science, where it can be utilized in the development of novel compounds with tailored properties. The compound's unique features, such as its ability to act as a building block for diverse chemical entities, make it an essential tool for those engaged in innovative research and product development.

Synonyms
5-(benciloxi)-1 H -indol-3-carbaldehído, 5-Benciloxi-3-formilindol
CAS Number
6953-22-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C16H13NO2
Molecular Weight
251.28
MDL Number
MFCD00014562
PubChem ID
81398
Melting Point
233-239 ?C
Appearance
Polvo amarillento
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
5-(benciloxi)-1 H -indol-3-carbaldehído, 5-Benciloxi-3-formilindol
CAS Number
6953-22-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C16H13NO2
Molecular Weight
251.28
MDL Number
MFCD00014562
PubChem ID
81398
Melting Point
233-239 ?C
Appearance
Polvo amarillento
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-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.
  • Pharmaceutical Research: It is explored for its potential therapeutic effects, particularly in developing new drugs targeting cancer and neurological disorders.
  • Fluorescent Probes: The compound can be modified to create fluorescent probes used in biological imaging, helping researchers visualize cellular processes.
  • Material Science: In the development of organic light-emitting diodes (OLEDs), this chemical can be incorporated into materials that enhance light emission efficiency.
  • Biochemical Studies: It is used in studies examining enzyme interactions and metabolic pathways, providing insights into biological functions and disease mechanisms.

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