61989-29-5

Usage

General Description

1H-Indole-3-acetic acid, 2,3-dihydro-2-oxo-, methyl ester, is a chemical compound with the formula C11H11NO3. It is a derivative of the plant hormone indole-3-acetic acid (IAA), which plays a crucial role in the regulation of plant growth and development. The methyl ester form of 1H-Indole-3-acetic acid can be used to study the biological activities and physiological effects of IAA in plants. It is commonly used in research and experimental settings to investigate the role of IAA in plant biology and to understand the mechanisms underlying plant growth and development. 1H-Indole-3-acetic acid, 2,3-dihydro-2-oxo-, methyl ester has potential applications in agriculture and horticulture for the regulation of plant growth and the enhancement of crop yield.

Upstream product

• 67-56-1 methanol 
• 2971-31-5 2,3-dihydro-2-oxo-1H-indole-3-acetic acid 
• 624-49-7 dimethylfumarate 
• 191171-55-8 2-anilineboronic acid pinacol ester 

Downstream Products

• 1304075-31-7 methyl (R)-2-[3-((1S)-3-oxocyclohexyl)-2-oxoindol-3-yl]acetate 
• 78941-89-6 2-oxo-1,2,3,4-tetrahydroquinoline-4-carboxylic acid methyl ester 
• 864924-14-1 (3aS,8aS,1'S)-(-)-bis(3-methyl-2-buten-1-yl)-2-oxo-1-(1'-phenylethyl)-2,3,3a,8a-tetrahydro-8H-pyrrolo[2,3-b]indole 
• 864924-15-2 (3aR,8aR,1'S)-(-)-bis(3-methyl-2-buten-1-yl)-2-oxo-1-(1'-phenylethyl)-2,3,3a,8a-tetrahydro-8H-pyrrolo[2,3-b]indole 

Relevant academic research and scientific papers

Convergent synthesis of dihydroquinolones from o-aminoarylboronates

An efficient and convergent one-step synthesis of substituted dihydroquinolin-2-ones from α,β-unsaturated esters and aminoaryl pinacolboronates under rhodium catalysis is reported. The reaction is easily applicable in parallel synthesis format and provide

Structural characterization of isomeric methyl 2-(2-oxo-3-indolyl)acetate and methyl 1-(2-oxo-4-quinolyl)formate

Crystalline and amorphous forms of methyl 2-(2-oxo-3-indolyl)acetate (1) were obtained showing significant differences in their melting points. The X-ray structure for the trigonal polymorph is reported. In addition, oxindole (1) was easily acid-catalyzed ring enlarged to give the structural isomer quinolone (2) for which the crystal structure was also determined. These results resolve several chemical inquiries related to the structural characterization of 1 and 2.