1360148-45-3

Upstream product

• 1360148-54-4 1-(4-methoxy-benzyl)-5-methyl-1H-indole-2-carboxylic acid ethyl ester 
• 1360148-58-8 [1-(4-methoxy-benzyl)-5-methyl-1H-indol-2-yl]-methanol 
• 1360148-62-4 1-(4-methoxy-benzyl)-5-methyl-1H-indole-2-carbaldehyde 
• 1360148-42-0 1-[1-(4-methoxy-benzyl)-5-methyl-1H-indol-2-yl]-hex-5-en-1-ol 
• 108-24-7 acetic anhydride 
• 16382-15-3 5-methyl-1H-indole-2-carboxylic acid ethyl ester 
• 5858-28-6 5-methyl-2-nitrobenzaldehyde 
• 66424-92-8 5-methyl-2-nitrobenzyl alcohol 

Downstream Products

• 1360148-51-1 acetic acid 5-hydroxy-1-[1-(4-methoxy-benzyl)-5-methyl-1H-indol-2-yl]-hexyl ester 

Relevant academic research and scientific papers

Synthetic approaches to natural antioxidant benzastatin E, F and G analogues

For synthesis of benzastatin E, F and G analogues, the indole-2- carbaldehydes with or without substituents at C-5 position were prepared as key intermediates. Several synthetic attempts to achieve benzastatin E-G analogues were suggested using the indole-2-carbaldehyde intermediates.