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Catalog Number:
26667
CAS Number:
23872-23-3
4-Cloro-2-oxoindolina-3-carbaldehído
Purity:
≥ 95% (RMN)
Documents
$96.34 /100 mg
Tamaño
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Product Information

4-Chloro-2-oxoindoline-3-carbaldehyde is a versatile compound recognized for its significant applications in organic synthesis and pharmaceutical development. This compound, also known as 4-Chloro-2-oxoindole-3-carbaldehyde, features a unique structure that allows it to serve as a valuable intermediate in the synthesis of various bioactive molecules. Researchers and industry professionals utilize this compound in the development of novel pharmaceuticals, particularly in the creation of indole-based derivatives that exhibit promising biological activities, including anti-cancer and anti-inflammatory properties.

Additionally, its reactivity and functional groups make it an ideal candidate for further modifications, enabling the design of tailored compounds for specific applications. The compound's stability and ease of handling further enhance its appeal in laboratory settings, making it a preferred choice for chemists engaged in synthetic research. With its potential to contribute to advancements in medicinal chemistry, 4-Chloro-2-oxoindoline-3-carbaldehyde stands out as a key player in the development of innovative therapeutic agents.

CAS Number
23872-23-3
Purity
≥ 95% (RMN)
Molecular Formula
C9H6ClNO2
Molecular Weight
195.6
MDL Number
MFCD20502958
PubChem ID
45791292
Appearance
Sólido amarillo claro
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
23872-23-3
Purity
≥ 95% (RMN)
Molecular Formula
C9H6ClNO2
Molecular Weight
195.6
MDL Number
MFCD20502958
PubChem ID
45791292
Appearance
Sólido amarillo claro
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

4-Chloro-2-oxoindoline-3-carbaldehyde is widely utilized in research focused on:

  • Synthetic Organic Chemistry: This compound serves as a versatile building block in the synthesis of various indole derivatives, which are important in the development of pharmaceuticals.
  • Drug Development: It is used in the creation of potential drug candidates, particularly in the field of anti-cancer and anti-inflammatory agents, due to its unique structural properties.
  • Fluorescent Probes: The compound can be modified to create fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes.
  • Material Science: It is applied in the formulation of advanced materials, such as organic light-emitting diodes (OLEDs), enhancing the performance of electronic devices.
  • Biochemical Research: The compound acts as a key reagent in various biochemical assays, helping scientists understand enzyme mechanisms and interactions in biological systems.

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