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Catalog Number:
17511
CAS Number:
98081-84-6
Éster metílico del ácido 6-cloro-1 H -indol-2-carboxílico
Purity:
≥ 98,5 % (HPLC)
Synonym(s):
6-cloro- 1H- indol-2-carboxilato de metilo
Documents
$93.14 /100 mg
Tamaño
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Product Information

6-Chloro-1H-indole-2-carboxylic acid methyl ester is a versatile compound widely recognized for its applications in pharmaceutical research and organic synthesis. This compound features a chloro-substituted indole structure, which is pivotal in the development of various bioactive molecules. Its unique properties make it an essential building block in the synthesis of indole derivatives, which are known for their diverse biological activities, including anti-inflammatory and anticancer properties. Researchers often utilize this compound in the synthesis of novel pharmaceuticals, agrochemicals, and other functional materials, leveraging its reactivity and stability to create complex molecular architectures.

In addition to its synthetic utility, 6-Chloro-1H-indole-2-carboxylic acid methyl ester serves as a valuable intermediate in the production of dyes and pigments, contributing to advancements in materials science. Its ability to undergo various chemical transformations allows for the exploration of new compounds with enhanced performance characteristics. With its broad range of applications, this compound is an excellent choice for researchers and industry professionals looking to innovate and develop new products in the fields of medicinal chemistry and materials development.

Synonyms
6-cloro- 1H- indol-2-carboxilato de metilo
CAS Number
98081-84-6
Purity
≥ 98,5 % (HPLC)
Molecular Formula
C10H8ClNO2
Molecular Weight
209.63
MDL Number
MFCD04966992
PubChem ID
4715032
Appearance
Sólido de color amarillo a naranja
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
6-cloro- 1H- indol-2-carboxilato de metilo
CAS Number
98081-84-6
Purity
≥ 98,5 % (HPLC)
Molecular Formula
C10H8ClNO2
Molecular Weight
209.63
MDL Number
MFCD04966992
PubChem ID
4715032
Appearance
Sólido de color amarillo a naranja
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

6-Chloro-1H-indole-2-carboxylic acid methyl ester is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly those targeting neurological disorders.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, contributing to the development of effective herbicides and fungicides that enhance crop yields.
  • Biochemical Research: Researchers employ this compound in studies related to enzyme inhibition and receptor binding, aiding in the discovery of new therapeutic agents.
  • Material Science: It finds applications in developing advanced materials, including polymers and coatings, due to its unique chemical properties.
  • Analytical Chemistry: The compound is utilized in various analytical techniques, such as chromatography, to separate and identify complex mixtures in research settings.

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