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Catalog Number:
20288
CAS Number:
552866-98-5
4-fluoro-2,3-dihydro-1 H -indole
Purity:
≥ 98% (CG)
Synonym(s):
4-Fluoroindoline
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$100.05 /250 mg
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Product Information

4-Fluoro-2,3-dihydro-1H-indole is a versatile chemical compound that has garnered attention in various fields, particularly in medicinal chemistry and pharmaceutical research. This compound is recognized for its unique structural features, which contribute to its potential as a building block in the synthesis of bioactive molecules. Its fluorine substituent enhances lipophilicity, making it an attractive candidate for drug development, especially in the creation of novel therapeutic agents targeting neurological disorders and cancer.

Researchers have utilized 4-Fluoro-2,3-dihydro-1H-indole in the synthesis of indole derivatives, which are known for their diverse biological activities, including anti-inflammatory and anti-cancer properties. The compound's ability to serve as a precursor in the development of complex organic molecules makes it invaluable for scientists looking to innovate in drug discovery. Its favorable reactivity and compatibility with various synthetic methodologies further enhance its appeal in both academic and industrial settings, paving the way for advancements in therapeutic solutions.

Synonyms
4-Fluoroindoline
CAS Number
552866-98-5
Purity
≥ 98% (CG)
Molecular Formula
C 8 H 8 FN
Molecular Weight
137.16
MDL Number
MFCD07371634
PubChem ID
16244440
Appearance
Liquide incolore
Conditions
Conserver à 0-8°C
General Information
Synonyms
4-Fluoroindoline
CAS Number
552866-98-5
Purity
≥ 98% (CG)
Molecular Formula
C 8 H 8 FN
Molecular Weight
137.16
MDL Number
MFCD07371634
PubChem ID
16244440
Appearance
Liquide incolore
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-Fluoro-2,3-dihydro-1H-indole is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly in the development of new drugs targeting neurological disorders.
  • Material Science: It is used in the creation of advanced materials, including polymers and coatings, which benefit from its unique chemical properties, enhancing durability and performance.
  • Biological Research: Researchers employ this compound to study its interactions with biological systems, aiding in the understanding of receptor binding and enzyme activity.
  • Agricultural Chemistry: It finds applications in the formulation of agrochemicals, contributing to the development of more effective pesticides and herbicides with reduced environmental impact.
  • Analytical Chemistry: The compound is utilized as a standard in analytical methods, improving the accuracy of chemical analyses in various samples.

Citations