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Catalog Number:
22041
CAS Number:
942-24-5
Méthyl indole-3-carboxylate
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ester méthylique de l'acide 1H-indole-3-carboxylique, 3-Carbométhoxyindole
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Product Information

Methyl indole-3-carboxylate is a versatile chemical compound widely recognized for its applications in organic synthesis and pharmaceutical development. This compound, also known as methyl 1H-indole-3-carboxylate, features a unique indole structure that enhances its reactivity and functionalization potential. Its properties make it an essential intermediate in the synthesis of various bioactive molecules, including pharmaceuticals and agrochemicals. Researchers often utilize methyl indole-3-carboxylate in the development of novel compounds with potential therapeutic effects, particularly in the fields of cancer research and neuropharmacology.

The compound's ability to undergo various chemical transformations allows for the creation of diverse derivatives, expanding its utility in medicinal chemistry. Its favorable solubility and stability further enhance its appeal for laboratory applications. Methyl indole-3-carboxylate stands out in the realm of indole derivatives due to its ease of synthesis and the broad range of potential applications, making it a valuable asset for researchers and industry professionals alike.

Synonyms
Ester méthylique de l'acide 1H-indole-3-carboxylique, 3-Carbométhoxyindole
CAS Number
942-24-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 10 H 9 NO 2
Molecular Weight
175.19
MDL Number
MFCD00189407
PubChem ID
589098
Melting Point
149-152 ?C
Appearance
Poudre cristalline blanc cassé
Conditions
Conserver à 0-8°C
General Information
Synonyms
Ester méthylique de l'acide 1H-indole-3-carboxylique, 3-Carbométhoxyindole
CAS Number
942-24-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 10 H 9 NO 2
Molecular Weight
175.19
MDL Number
MFCD00189407
PubChem ID
589098
Melting Point
149-152 ?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-3-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 Chemicals: It is used in the formulation of agrochemicals, providing effective solutions for pest control and plant growth regulation, thus improving crop yields.
  • Biochemical Research: Researchers employ this compound in studies related to enzyme inhibition and metabolic pathways, aiding in the understanding of complex biological systems.
  • Material Science: Methyl indole-3-carboxylate is incorporated in the development of novel polymers and materials, contributing to advancements in coatings and adhesives with enhanced properties.
  • Flavor and Fragrance Industry: Its unique aromatic properties make it a valuable ingredient in the formulation of flavors and fragrances, offering a natural alternative to synthetic compounds.

Citations