1418136-25-0

Basic information

• Product Name: 2-bromo-5-(4-methoxyphenyl)-1H-indole
• Synonyms: 2-bromo-5-(4-methoxyphenyl)-1H-indole
• CAS NO: 1418136-25-0
• Molecular Weight: 302.17
• Mol File: 1418136-25-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-bromo-5-(4-methoxyphenyl)-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-5-(4-methoxyphenyl)-1H-indole(1418136-25-0)
• EPA Substance Registry System: 2-bromo-5-(4-methoxyphenyl)-1H-indole(1418136-25-0)

Safety Data

• Hazardous Substances Data: 1418136-25-0(Hazardous Substances Data)

Upstream product

• 144104-46-1 5-(4-methoxyphenyl)-1H-indole 
• 1418136-21-6 C₁₆H₁₅Br₂NO₃S 

Relevant articles and documents

Method for preparing 2-bromoindole by using electrochemical micro-channel device

The invention provides a method for preparing 2-bromoindole by using an electrochemical micro-channel device, which comprises the following steps: assembling an electrochemical micro-channel reactiondevice, and dissolving indole compounds and bromine-cont

The facile synthesis of 2-bromoindoles via Cs2CO 3-promoted intramolecular cyclization of 2-(gem-dibromovinyl)anilines under transition-metal-free conditions

2-Bromoindoles were readily prepared through a facile Cs2CO 3-promoted intramolecular cyclization of 2-(gem-bromovinyl)-N- methylsulfonylanilines in excellent yields under transition-metal-free conditions. This methodology could be extended to the synthesis of corresponding 2-chloroindoles. The reaction mechanism suggested that cyclization occurs through a key intermediate, phenylethynyl bromide, followed by cyclization in one-pot. The Royal Society of Chemistry.