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Catalog Number:
21364
CAS Number:
89434-04-8
4-Fluoroindole-3-acétonitrile
Purity:
≥ 97 % (HPLC)
Synonym(s):
4-Fluoro-3-indoleacétonitrile, (4-Fluoro-1 H -indol-3-yl)-acétonitrile
Documents
$173.66 /100 mg
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Product Information

4-Fluoroindole-3-acetonitrile is a versatile chemical compound recognized for its significant applications in pharmaceutical and chemical research. This compound, characterized by its unique fluorine substitution, serves as a valuable intermediate in the synthesis of various bioactive molecules. Its structure allows for enhanced reactivity, making it a crucial building block in the development of novel pharmaceuticals, particularly in the field of medicinal chemistry where it can be utilized to create compounds with improved efficacy and selectivity.

Researchers and industry professionals appreciate 4-Fluoroindole-3-acetonitrile for its potential in the synthesis of indole derivatives, which are known for their diverse biological activities, including anti-cancer and anti-inflammatory properties. The compound's ability to facilitate complex chemical reactions positions it as a key player in drug discovery and development processes. Its unique properties not only streamline synthetic pathways but also enhance the overall yield of desired products, making it an essential tool for chemists aiming to innovate in their respective fields.

Synonyms
4-Fluoro-3-indoleacétonitrile, (4-Fluoro-1 H -indol-3-yl)-acétonitrile
CAS Number
89434-04-8
Purity
≥ 97 % (HPLC)
Molecular Formula
C 10 H 7 FN 2
Molecular Weight
174.18
MDL Number
MFCD04972070
PubChem ID
13499093
Appearance
Poudre cristalline jaunâtre à blanc cassé
Conditions
Conserver à 0-8 °C
General Information
Synonyms
4-Fluoro-3-indoleacétonitrile, (4-Fluoro-1 H -indol-3-yl)-acétonitrile
CAS Number
89434-04-8
Purity
≥ 97 % (HPLC)
Molecular Formula
C 10 H 7 FN 2
Molecular Weight
174.18
MDL Number
MFCD04972070
PubChem ID
13499093
Appearance
Poudre cristalline jaunâtre à blanc cassé
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

4-Fluoroindole-3-acetonitrile is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.
  • Material Science: It is used in the development of advanced materials, such as organic semiconductors, due to its unique electronic properties, which can lead to improved performance in electronic devices.
  • Biochemical Research: Researchers leverage its structure to study enzyme interactions and signaling pathways, aiding in the understanding of complex biological systems.
  • Fluorescent Probes: The compound can be modified to create fluorescent probes for imaging applications in cellular biology, allowing for real-time observation of cellular processes.
  • Agrochemical Formulations: It is explored in the formulation of agrochemicals, where its properties can enhance the effectiveness of crop protection agents, contributing to sustainable agriculture.

Citations