150308-11-5

Upstream product

• 5165-56-0 1-(4-methylphenyl)-3-acetyl-5-hydroxy-2-methylindole 

Downstream Products

• 157064-71-6 (3-Acetyl-6-bromo-2-methyl-1-p-tolyl-1H-indol-5-yloxy)-acetic acid ethyl ester 
• 171112-40-6 1-(6-Bromo-5-methoxy-2-methyl-1-p-tolyl-1H-indol-3-yl)-ethanone 
• 171112-44-0 2-Bromo-1-(6-bromo-5-methoxy-2-methyl-1-p-tolyl-1H-indol-3-yl)-ethanone 
• 157064-79-4 (3-Acetyl-6-bromo-2-methyl-1-p-tolyl-1H-indol-5-yloxy)-acetic acid hydrazide 
• 157065-11-7 C₂₇H₂₅BrN₄O₃S 

Relevant academic research and scientific papers

SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF 4-ISO-GRAMINES, 4-ARYL-THIOMETHYL AND 3-AMINOACETYL DERIVATIVES OF 2-METHYLINDOLES

1-Substituted-2-methyl-3-acetyl-5-hydroxy-indoles are subjected to Mannich reaction to give exclusively 4-isogramines.Futher, these 4-dimethylaminomethyl-5-hydroxyindoles are reacted with thiophenols to yield the corresponding 4-arylthiomethyl-5-hydroxyin

Synthesis and antimicrobial activity of furoindole derivatives

8-Bromofuroindole derivatives (5a-d) have been prepared by cyclodehydration of 5-benzoylmethoxy-6-bromoindoles (4a-d) with PPA at 90-100 deg C. 3,6-Diacetyl-5-hydroxyindoles (6a-c) on reaction with ethyl chloroacetate followed by hydrolysis with aq