16712-58-6

Usage

Uses

Used in Plastic Industry:
5-Amino-2,3-dimethylindole is used as a dye precursor for the creation of spectrally pure dyes in the plastic industry. These dyes are essential for producing plastics with specific color properties, enhancing their visual appeal and functionality.
Used in Paint Industry:
In the paint industry, 5-Amino-2,3-dimethylindole is used as a dye intermediate to develop spectrally pure dyes. These dyes contribute to the formulation of paints with a wide range of colors, ensuring a diverse selection for various applications, such as interior and exterior coatings.
Used in Textile Industry:
5-Amino-2,3-dimethylindole is employed as a dye component in the textile industry. The dyes derived from 5-AMINO-2,3-DIMETHYLINDOLE are used to color fabrics, providing a broad spectrum of hues and shades for clothing, home textiles, and other textile products. 5-AMINO-2,3-DIMETHYLINDOLE plays a vital role in the production of vibrant and long-lasting colors in textiles.

InChI:InChI=1/C10H12N2/c1-6-7(2)12-10-4-3-8(11)5-9(6)10/h3-5,12H,11H2,1-2H3

Upstream product

• 21296-94-6 2,3-Dimethyl-5-nitro-1H-indole 
• 91-55-4 2,3-dimethylindole 
• 1017-79-4 butan-2-one-(4-nitro-phenylhydrazone) 
• 100-01-6 4-nitro-aniline 
• 100-16-3 4-nitrophenylhydrazone 

Downstream Products

• 119040-09-4 6,7-dimethyl-2,3-diphenyl-1H,5H-pyrrolo<2,3-f>indole 
• 119014-21-0 7,8-dimethyl-1,2-diphenyl-3H,6H-pyrrolo<3,2-e>indole 
• 852067-94-8 C₂₀H₁₉ClN₄O₂ 
• 1063625-20-6 8,9-dimethyl-2,4-diphenyl-7H-pyrrolo[2,3-h]quinoline 
• 64498-81-3 7,9-Diphenyl-1,2-dimethylpyrrolo<3.2-f>quinoline 
• 1338222-28-8 N'-[1-(2-chloro-6-fluoro-benzyl)-2,3-dimethyl-1H-indol-5-yl]-N-ethyl-N-methyl-formamidine 
• 852333-67-6 {6-[2-(3,4-dimethoxy-phenyl)-ethoxy]-4-morpholin-4-yl-pyridin-2-yl}-(2,3-dimethyl-1H-indol-5-yl)-amine 

Relevant academic research and scientific papers

INDOLE COMPOUNDS FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES

Methods of treating polyQ diseases or disorders such as Huntington's Disease are presented. Compounds of formula (I) of the disclosure are capable of binding directly to the polyQ segment of mutated huntingtin. This binding results in at least partial rev

One-pot synthesis of pyrrolo[3,2-f]-and pyrrolo[2,3-h]quinoline derivatives: Observation of an unexpected mechanistic pathway

One-pot synthesis of pyrrolo[3,2-f]- and pyrrolo[2,3-h]quinolines were obtained starting from substituted 5-aminoindoles, benzaldehydes, and phenylacetylenes in the presence of La(OTf)3 as a catalyst in good yields. The indole moiety in 5-aminoindole is believed to be mainly responsible for the observation of unexpected mechanistic pathway to the formation of pyrrolo[2,3-h]quinoline. Georg Thieme Verlag Stuttgart · New York.