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Catalog Number:
22064
CAS Number:
50820-65-0
Méthyl indole-6-carboxylate
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ester méthylique de l'acide indole-6-carboxylique
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Product Information

Methyl Indole-6-carboxylate is a versatile compound widely recognized for its applications in organic synthesis and medicinal chemistry. This ester derivative of indole features a methyl group and a carboxylate functional group, making it an essential building block in the synthesis of various bioactive molecules. Its unique structure allows for the development of compounds with potential pharmaceutical properties, particularly in the fields of anti-inflammatory and anticancer research. Researchers often utilize Methyl Indole-6-carboxylate in the synthesis of indole-based derivatives, which are known for their diverse biological activities, including antimicrobial and antioxidant effects.

In addition to its synthetic utility, Methyl Indole-6-carboxylate serves as a valuable intermediate in the production of agrochemicals and dyes, showcasing its relevance across multiple industries. Its favorable reactivity and compatibility with various reaction conditions make it an attractive choice for chemists looking to innovate in drug discovery and development. With its broad range of applications and potential benefits, Methyl Indole-6-carboxylate stands out as a compound of interest for both researchers and industry professionals.

Synonyms
Ester méthylique de l'acide indole-6-carboxylique
CAS Number
50820-65-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 10 H 9 NO 2
Molecular Weight
175.19
MDL Number
MFCD00211063
PubChem ID
639844
Melting Point
75-84º C
Appearance
Poudre cristalline blanc cassé
Conditions
Conserver à 0-8°C
General Information
Synonyms
Ester méthylique de l'acide indole-6-carboxylique
CAS Number
50820-65-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 10 H 9 NO 2
Molecular Weight
175.19
MDL Number
MFCD00211063
PubChem ID
639844
Melting Point
75-84º C
Appearance
Poudre cristalline blanc cassé
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

Methyl Indole-6-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, contributing to the development of effective pesticides and herbicides that are safer for the environment.
  • Biochemical Research: Researchers employ this compound in studies related to enzyme inhibition and receptor interactions, aiding in the understanding of biological pathways and disease mechanisms.
  • Material Science: Methyl Indole-6-carboxylate is explored in the development of novel materials, including polymers and coatings, which offer improved durability and performance.
  • Flavor and Fragrance Industry: This chemical is also utilized in creating flavoring agents and fragrances, providing unique aromatic properties that enhance consumer products.

Citations