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Catalog Number:
24321
CAS Number:
16792-45-3
6-nitro-1 H -indole-2-carboxylate d'éthyle
Purity:
≥ 98 % (HPLC)
Documents
$60.00 /100 mg
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Product Information

Ethyl 6-nitro-1H-indole-2-carboxylate is a versatile compound widely recognized for its applications in organic synthesis and medicinal chemistry. This compound features a nitro group that enhances its reactivity, making it an excellent intermediate for the synthesis of various biologically active molecules. Researchers often utilize Ethyl 6-nitro-1H-indole-2-carboxylate in the development of pharmaceuticals, particularly in the creation of indole derivatives that exhibit significant anti-inflammatory and anticancer properties. Its ability to participate in diverse chemical reactions, such as nucleophilic substitutions and cycloadditions, further underscores its utility in synthetic chemistry.

In addition to its role in drug development, Ethyl 6-nitro-1H-indole-2-carboxylate is also employed in the production of agrochemicals and dyes, showcasing its broad applicability across different industries. The compound's unique structure allows for modifications that can lead to enhanced biological activity, making it a valuable asset for researchers aiming to innovate in the fields of medicinal and agricultural chemistry. With its proven track record and potential for further exploration, Ethyl 6-nitro-1H-indole-2-carboxylate stands out as a key player in advancing chemical research and development.

CAS Number
16792-45-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C11H10N2O4
Molecular Weight
234.21
MDL Number
MFCD04973967
PubChem ID
616444
Appearance
Solide jaune
Conditions
Conserver à 0-8 °C
General Information
CAS Number
16792-45-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C11H10N2O4
Molecular Weight
234.21
MDL Number
MFCD04973967
PubChem ID
616444
Appearance
Solide 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

Ethyl 6-nitro-1H-indole-2-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and analgesic drugs.
  • Organic Synthesis: It is used in organic chemistry for the construction of complex molecules, enabling researchers to create new compounds with potential therapeutic effects.
  • Biological Research: The compound is studied for its biological activity, including its effects on cellular processes, making it valuable in drug discovery and development.
  • Material Science: Ethyl 6-nitro-1H-indole-2-carboxylate is explored for its potential applications in creating novel materials, such as polymers with enhanced properties.
  • Agricultural Chemistry: It has potential uses in developing agrochemicals, contributing to the formulation of effective pesticides or herbicides that target specific pests while minimizing environmental impact.

Citations