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Catalog Number:
17482
CAS Number:
20870-77-3
4-Chloro-1,3-dihydroindol-2-one
Purity:
≥ 98 % (HPLC)
Synonym(s):
4-Chloro-2-oxindole
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Product Information

4-Chloro-1,3-dihydroindol-2-one is a versatile compound known for its unique chemical structure and properties, making it valuable in various research and industrial applications. This compound is recognized for its potential as a building block in the synthesis of pharmaceuticals, particularly in the development of indole-based derivatives that exhibit biological activity. Its ability to act as an intermediate in organic synthesis allows researchers to explore new pathways for drug discovery and development.

Additionally, 4-Chloro-1,3-dihydroindol-2-one has been utilized in the formulation of agrochemicals, where it contributes to the design of effective herbicides and fungicides. Its stability and reactivity make it an attractive option for chemists looking to create innovative solutions in both medicinal and agricultural chemistry. With its favorable properties, this compound stands out as a key ingredient for professionals aiming to enhance their research outcomes or product formulations.

Synonyms
4-Chloro-2-oxindole
CAS Number
20870-77-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C8H6ClNO
Molecular Weight
167.59
MDL Number
MFCD03787567
PubChem ID
1480686
Appearance
Poudre blanc cassé à jaune
Conditions
Conserver à 0-8 °C
General Information
Synonyms
4-Chloro-2-oxindole
CAS Number
20870-77-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C8H6ClNO
Molecular Weight
167.59
MDL Number
MFCD03787567
PubChem ID
1480686
Appearance
Poudre blanc cassé à jaune
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-Chloro-1,3-dihydroindol-2-one is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in creating anti-inflammatory and analgesic drugs.
  • Organic Synthesis: It is employed in organic chemistry for the development of complex molecules, offering a versatile building block for researchers aiming to create novel compounds.
  • Biological Research: The compound is used in studies investigating its biological activity, including potential anticancer properties, making it valuable for researchers in medicinal chemistry.
  • Material Science: It finds applications in the development of new materials, such as polymers and coatings, due to its unique chemical properties that enhance material performance.
  • Analytical Chemistry: 4-Chloro-1,3-dihydroindol-2-one is utilized in analytical methods for detecting and quantifying other compounds, aiding in quality control processes in various industries.

Citations