1173282-83-1

Basic information

• Product Name: [(5-bromo-1H-indol-3-yl)-(4-chlorophenyl)-methyl]-methyl-phenyl-amine
• Synonyms: [(5-bromo-1H-indol-3-yl)-(4-chlorophenyl)-methyl]-methyl-phenyl-amine
• CAS NO: 1173282-83-1
• Molecular Weight: 425.755
• Mol File: 1173282-83-1.mol

Chemical Properties

• CAS DataBase Reference: [(5-bromo-1H-indol-3-yl)-(4-chlorophenyl)-methyl]-methyl-phenyl-amine(CAS DataBase Reference)
• NIST Chemistry Reference: [(5-bromo-1H-indol-3-yl)-(4-chlorophenyl)-methyl]-methyl-phenyl-amine(1173282-83-1)
• EPA Substance Registry System: [(5-bromo-1H-indol-3-yl)-(4-chlorophenyl)-methyl]-methyl-phenyl-amine(1173282-83-1)

Safety Data

• Hazardous Substances Data: 1173282-83-1(Hazardous Substances Data)

Upstream product

• 10075-50-0 5-bromo-1H-indole 
• 104-88-1 4-chlorobenzaldehyde 
• 100-61-8 N-methylaniline 
• 873-76-7 para-Chlorobenzyl alcohol 

Relevant articles and documents

One-pot synthesis of 3-[(N-alkylanilino)(aryl)methyl]indoles via a transition metal assisted three-component condensation at room temperature

A simple and highly efficient protocol for the one-pot synthesis of a series of 3-[(N-alkylanilino)(aryl)methyl]indoles has been developed based on low-cost and environmentally benign zirconium oxychloride octahydrate and copper chloride dihydrate catalysts via three-component condensation between indoles, aromatic aldehydes, and N-alkylanilines at room temperature under neat condition. Mild reaction conditions, operational simplicity, high atom-economy, good yields in relatively shorter reaction times, use of low-cost and eco-friendly catalysts are some of the salient features of this protocol. A simple and highly efficient protocol for the one-pot synthesis of a series of 3-[(N-alkylanilino)(aryl)methyl]indoles has been developed based on low-cost and environmentally benign zirconium oxychloride octahydrate and copper chloride dihydrate catalysts via three-component condensation between indoles, aromatic aldehydes, and N-alkylanilines at room temperature under neat condition. Mild reaction conditions, operational simplicity, high atom-economy, good yields in relatively shorter reaction times, and use of low-cost and eco-friendly catalysts are the key advantages of the present protocol.

Iron mediated one pot three component synthesis of 3-substituted indoles via aerobic iminium ion formation

An efficient and economical method was developed for the synthesis of 3 substituted indoles by a highly efficient one-pot three component coupling reaction of substituted or unsubstituted benzyl alcohol, N-methyl aniline or pyrrolidine, and indoles or sub

PANI-HBF4: A reusable polymer-based solid acid catalyst for three-component, one-pot synthesis of 3-substituted amino methyl indoles under solvent-free conditions

A simple, fast, efficient, high-yielding, and green process is developed for one-pot, three-component synthesis of 3-substituted amino methyl indoles under solvent-free conditions using polyaniline salt as polymer-based reusable solid acid catalyst at room temperature. The advantages of polyaniline salt catalyst are ease of synthesis and handling, low cost, versatality, and recyclability. Copyright Taylor & Francis Group, LLC.

Zwitterionic-type molten salt: A mild and efficient organocatalyst for the synthesis of 3-aminoalkylated indoles via three-component coupling reaction

A general and efficient method has been developed for the synthesis of 3-aminoalkylated indoles by a three-component coupling of indoles, aldehydes, and amines in the presence of a catalytic amount of zwitterionic-type molten salt under solvent-free condi

One-pot three-component coupling reaction: solvent-free synthesis of novel 3-substituted indoles catalyzed by PMA-SiO2

Solvent-free PMA-SiO2-catalyzed synthesis of 3-substituted indole derivatives by a one-pot three-component coupling reaction between aldehyde, N-methyl aniline and indole is described.