105776-29-2

Upstream product

• 70-11-1 α-bromoacetophenone 
• 10272-07-8 3.5-dimethoxyaniline 
• 1046806-68-1 4,6-dimethoxy-3-phenyl-1-acetylindole 
• 1046806-74-9 N-acetyl-2-(4,6-dimethoxyphenylamino)-1-phenylethanone 
• 74794-87-9 2-<(3,5-dimethoxyphenyl)amino>-1-phenylethanone 

Downstream Products

• 426255-80-3 1-(4,6-dimethoxy-3-phenylindol-2-yl)-3-phenylprop-2-en-1-one 
• 1359077-25-0 1,2-di(4,6-dimethoxy-3-phenylindol-1-ylmethyl)benzene 
• 1359077-26-1 2-(4-chlorophenyl)-6,8,23,25-tetramethoxy-4,27-diphenyl-11,20-diazaheptacyclo[18,7,0,0(1,20),0(3,11),0(5,10),0(13,18),0(21,26)]heptadoaconta-1⁽²⁷⁾,3,5,7,9,13,15,17,21,23,25-undecaene 
• 151320-88-6 4,6-dimethoxy-3-phenylindole-2,7-dicarbaldehyde 
• 1238398-72-5 5,7-dimethoxy-2,3-dihydro-1-[4,6-dimethoxy-3-phenylindol-2-yl]-1,3,3-trimethyl-4-phenyl-1H-pyrrolo[1,2-a]indole 
• 1159837-08-7 C₃₂H₂₈N₂O₄ 
• 1146074-12-5 N,N-dimethyl-4,6-dimethoxy-3-phenylindol-1-ylacetamide 
• 1100050-18-7 methyl 4,6-dimethoxy-3-phenylindol-1-ylacetate 
• 1048988-04-0 N-(methanesulfonyl)-4,6-dimethoxy-3-phenylindole 
• 1046806-66-9 1-(4',6'-dimethoxy-3'-phenylindol-7-yl)-2,2,2-trifluoroethanone 
• 151321-08-3 [2-[2-Hydroxymethyl-4,6-dimethoxy-3-(4-methoxy-phenyl)-1H-indol-7-ylmethyl]-4,6-dimethoxy-3-(4-methoxy-phenyl)-1H-indol-7-yl]-methanol 
• 151321-06-1 C₃₇H₃₄N₂O₈ 

Relevant academic research and scientific papers

Dimethoxyindoles based thiosemicarbazones as multi-target agents; synthesis, crystal interactions, biological activity and molecular modeling

Alzheimer's disease (AD) is known as one of the most devastating neurodegenerative disease diagnosed for the old-aged people and cholinesterase inhibitors (ChEI) can be used as an effective palliative treatment for AD. A range of novel monomeric and dimer

First heterogeneous ligand- and salt-free larock indole Synthesis

A new ligand- and salt-free procedure using heterogeneous palladium catalysts for the Larock indole and benzofuran synthesis is reported. After optimisation of the reaction conditions, good to high isolated yields have been achieved for a variety of structures. Recycling studies have shown that the palladium catalysts can be readily recovered and reused. Reactions and recovery of the palladium catalysts can be carried out in the presence of air, without any particular precaution.

Synthesis of activated 3-substituted indoles: An optimised one-pot procedure

3-Substituted-4,6-dimethoxyindoles can be synthesised in a one-pot procedure from 3,5-dimethoxyaniline and 2-haloketones in the presence of lithium bromide and sodium bicarbonate. Graphical Abstract.

Synthesis of Activated 3-Arylindoles

A wide range of substituted 3-aryl-4,6-dimethoxyindoles (6) has been synthesized from the related α-anilinoacetophenones (5), in which the nitrogen atom is protected by a trifluoroacetyl or acetyl group.This method has led to the synthesis of a 3,7'-biindolyl (12).

Synthesis of 4,6-Dimethoxyindoles

Syntheses are described for nine new 4,6-dimethoxyindoles, incorporating phenyl, pyridin-2-yl, methoxycarbonyl, carboxy and methyl groups in the 2- and/or 3-positions.