1040308-67-5

Basic information

• Product Name: N-(2-bromobenzyl)-2-iodoaniline
• Synonyms: N-(2-bromobenzyl)-2-iodoaniline
• CAS NO: 1040308-67-5
• Molecular Weight: 388.046
• Mol File: 1040308-67-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(2-bromobenzyl)-2-iodoaniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-bromobenzyl)-2-iodoaniline(1040308-67-5)
• EPA Substance Registry System: N-(2-bromobenzyl)-2-iodoaniline(1040308-67-5)

Safety Data

• Hazardous Substances Data: 1040308-67-5(Hazardous Substances Data)

Upstream product

• 615-43-0 2-iodophenylamine 
• 6630-33-7 ortho-bromobenzaldehyde 

Downstream Products

• 1364806-24-5 6-(phenylsulfonyl)-5,12-dihydroindolo[2,1-b]quinazoline 
• 1364806-37-0 2-amino-1-(2-bromobenzyl)-1H-indole-3-carbonitrile 
• 1451735-25-3 C₂₂H₁₄BrNO 
• 1451735-26-4 C₃₃H₃₇BrN₄O₂ 
• 23194-93-6 (Z)-5,6-dihydrodibenzo[b,f]azocine 

Relevant articles and documents

Bis(dibenzylideneacetone)palladium(0)/tert-Butyl Nitrite- Catalyzed Cyclization of o-Alkynylanilines with tert-Butyl Nitrite: Synthesis and Applications of Indazole 2-Oxides

An efficient method for the synthesis of 1-benzyl/arylindazole 2-oxides via a bis(dibenzylideneacetone)palladium(0) [Pd(dba)2]/tert-butyl nitrite (TBN)-catalyzed reaction of o-alkynylaniline derivatives with TBN is reported. The overall transfo

A facile copper-catalyzed one-pot domino synthesis of 5,12-dihydroindolo[2, 1- b ]quinazolines

A domino synthesis of 5,12-dihydroindolo[2,1-b]quinazoline derivatives via copper-catalyzed Ullmann-type intermolecular C-C and intramolecular C-N couplings is reported. Good yields of various 5,12-dihydroindolo[2,1-b] quinazoline derivatives were obtained. Reaction scopes, limitations, and the reaction mechanism are discussed.