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Usage

Uses

Used in Pharmaceutical Research:
Tert-Butyl (1-methyl-1H-indol-3-yl)carbamate is used as a reagent in pharmaceutical research for its potential medicinal properties. It has been studied for its anti-inflammatory and anti-cancer activities, making it a promising candidate for the development of new drugs.
Used in Organic Synthesis:
Tert-Butyl (1-methyl-1H-indol-3-yl)carbamate is used as a reagent in organic synthesis due to its unique structure and chemical properties. It can be used to synthesize various organic compounds and contribute to the advancement of chemical research.
Used in Insecticide and Pesticide Development:
As a carbamate derivative, Tert-Butyl (1-methyl-1H-indol-3-yl)carbamate may possess insecticidal or pesticidal properties. It can be used in the development of new insecticides and pesticides to control pests and protect crops.
Used in Scientific Research:
Due to its unique structure and potential applications, Tert-Butyl (1-methyl-1H-indol-3-yl)carbamate is of interest to researchers in various scientific fields. It can be used in studies to explore its properties and potential uses in different industries.

Upstream product

• 36728-89-9 1-methyl-3-nitro-1H-indole 
• 24424-99-5 di-tert-butyl dicarbonate 
• 64-19-7 acetic acid 
• 32387-21-6 1-methyl-3-indolecarboxylic acid 
• 75-65-0 tert-butyl alcohol 

Relevant academic research and scientific papers

TRIAZOLE AGONISTS OF THE APJ RECEPTOR

Compounds of Formula I and Formula II, pharmaceutically acceptable salt thereof, stereoisomers of any of the foregoing, or mixtures thereof are agonists of the APJ Receptor and have use in treating cardiovascular and other conditions. Compounds of Formula I and Formula II have the following structures where the definitions of the variables are provided herein.

Three-component reaction involving metal-free heteroannulation of N-Boc-3-amido indole, aryl aldehydes, and aromatic alkynes under microwave conditions: Synthesis of highly diversified δ-carbolines

An efficient synthesis toward highly diversified δ-carbolines via one-pot multicomponent reaction using N-Boc-3-amido indoles, aryl aldehydes, and aromatic terminal alkynes under microwave conditions has been described.

Efficient reductive acylation of 3-nitroindoles

3-Nitroindoles are catalytically reduced by hydrogen on palladium/carbon to furnish the relatively unstable aminoindoles, which in the presence of carboxylic acid anhydrides afford good to excellent yields of the corresponding N-acylaminoindoles. 2-Nitroi

Convenient synthesis of masked aminoindoles by indium mediated one-pot reductive acylation of 3- and 2-nitroindoles

Unstable 3- and 2-aminoindoles arc generated in situ by indium mediated reduction of 3- and 2-nitroindoles and capped as the stable amides (or carbamate) in moderate to high yields under mild conditions in a one-pot procedure.