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Catalog Number:
17303
CAS Number:
53995-82-7
Ester éthylique de l'acide 4,6-dichloro-1 H -indole-2-carboxylique
Purity:
≥ 98 % (HPLC)
Synonym(s):
4,6-dichloro-1 H -indole-2-carboxylate d'éthyle
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Product Information

4,6-Dichloro-1H-indole-2-carboxylic acid ethyl ester is a versatile compound known for its significant applications in pharmaceutical research and development. This compound features a unique dichlorinated indole structure, which enhances its reactivity and potential as a building block in the synthesis of various bioactive molecules. Its ethyl ester form provides improved solubility, making it an ideal candidate for drug formulation and delivery systems. Researchers have utilized this compound in the development of novel therapeutic agents, particularly in the fields of oncology and anti-inflammatory treatments, due to its ability to interact with biological targets effectively.

In addition to its pharmaceutical applications, 4,6-Dichloro-1H-indole-2-carboxylic acid ethyl ester serves as a valuable intermediate in organic synthesis, facilitating the creation of complex chemical structures. Its unique properties allow for the exploration of new chemical pathways, making it a preferred choice for chemists looking to innovate in their research. With its proven efficacy and adaptability, this compound holds great potential for advancing scientific discovery and improving therapeutic outcomes.

Synonyms
4,6-dichloro-1 H -indole-2-carboxylate d'éthyle
CAS Number
53995-82-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C11H9Cl2NO2
Molecular Weight
258.1
MDL Number
MFCD00800654
PubChem ID
2736407
Melting Point
181-191 ?C
Appearance
Solide jaune pâle
Conditions
Conserver à 0-8°C
General Information
Synonyms
4,6-dichloro-1 H -indole-2-carboxylate d'éthyle
CAS Number
53995-82-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C11H9Cl2NO2
Molecular Weight
258.1
MDL Number
MFCD00800654
PubChem ID
2736407
Melting Point
181-191 ?C
Appearance
Solide jaune pâle
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

4,6-Dichloro-1H-indole-2-carboxylic acid ethyl ester is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing drugs targeting cancer and infectious diseases.
  • Agricultural Chemicals: It is used in formulating agrochemicals, providing effective solutions for pest control and crop protection, thereby enhancing agricultural productivity.
  • Biochemical Research: Researchers employ this compound to study biochemical pathways and mechanisms, aiding in the discovery of new therapeutic targets.
  • Material Science: The compound is explored for its potential in creating novel materials with unique properties, such as conducting polymers and dyes.
  • Analytical Chemistry: It is utilized as a standard reference material in analytical methods, ensuring accuracy and reliability in chemical analysis.

Citations