91444-16-5

Basic information

• Product Name: 6-methoxy-2-(4-methoxyphenyl)-3-methyl-1H-indole
• Synonyms: 6-methoxy-2-(4-methoxyphenyl)-3-methyl-1H-indole
• CAS NO: 91444-16-5
• Molecular Weight: 267.327
• Mol File: 91444-16-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 6-methoxy-2-(4-methoxyphenyl)-3-methyl-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 6-methoxy-2-(4-methoxyphenyl)-3-methyl-1H-indole(91444-16-5)
• EPA Substance Registry System: 6-methoxy-2-(4-methoxyphenyl)-3-methyl-1H-indole(91444-16-5)

Safety Data

• Hazardous Substances Data: 91444-16-5(Hazardous Substances Data)

Upstream product

• 21086-33-9 2-bromo-1-(4-methoxyphenyl)-1-propanone 
• 536-90-3 m-Anisidine 
• 487003-20-3 1-benzyl-6-methoxy-1H-indole-2,3-dione 
• 52351-75-4 6-methoxyisatin 
• 104598-83-6 1-benzyl-6-methoxy-2-(4-methoxyphenyl)-3-methyl-1H-indole 

Downstream Products

• 158611-24-6 6-methoxy-2-(4-methoxyphenyl)-1H-indole-3-carbaldehyde 
• 86111-31-1 Acetic acid 2-(4-acetoxy-phenyl)-3-methyl-1-propyl-1H-indol-6-yl ester 
• 91444-57-4 Acetic acid 2-(4-acetoxy-phenyl)-1-isopropyl-3-methyl-1H-indol-6-yl ester 
• 86111-30-0 Acetic acid 2-(4-acetoxy-phenyl)-1-ethyl-3-methyl-1H-indol-6-yl ester 
• 86111-29-7 Acetic acid 2-(4-acetoxy-phenyl)-1,3-dimethyl-1H-indol-6-yl ester 
• 91444-50-7 Acetic acid 2-(4-acetoxy-phenyl)-3-methyl-1H-indol-6-yl ester 
• 86111-16-2 2-(4-Hydroxy-phenyl)-3-methyl-1-propyl-1H-indol-6-ol 
• 91444-56-3 2-(4-Hydroxy-phenyl)-1-isopropyl-3-methyl-1H-indol-6-ol 
• 86111-14-0 2-(4-Hydroxy-phenyl)-1,3-dimethyl-1H-indol-6-ol 
• 86111-15-1 1-Ethyl-2-(4-hydroxy-phenyl)-3-methyl-1H-indol-6-ol 
• 104599-19-1 Acetic acid 2-(4-acetoxy-phenyl)-1-benzyl-3-methyl-1H-indol-6-yl ester 
• 104599-35-1 Acetic acid 2-(4-acetoxy-phenyl)-3-methyl-1-phenyl-1H-indol-6-yl ester 
• 104599-01-1 1-Benzyl-2-(4-hydroxy-phenyl)-3-methyl-1H-indol-6-ol 
• 104599-17-9 2-(4-Hydroxy-phenyl)-3-methyl-1-phenyl-1H-indol-6-ol 

Relevant articles and documents

Divergent and Orthogonal Approach to Carbazoles and Pyridoindoles from Oxindoles via Indole Intermediates

The previously unexplored Grignard addition to oxindoles provides a regiospecific approach to 2- and 2,3-disubstituted indole derivatives in high yields via a one-pot aromatization driven dehydration pathway. This method allows a convenient preparation of diallyl indoles that are used as ring-closing metathesis (RCM) precursors for the orthogonal synthesis of pyrido[1,2-a]indoles and carbazoles. The synthetic utility of this method is illustrated by the synthesis of a microtubulin inhibitor and naturally occurring carbazole alkaloids.