861609-74-7

Basic information

• Product Name: 2-chloro-6-iodo-4-nitroaniline
• Synonyms: 2-chloro-6-iodo-4-nitroaniline
• CAS NO: 861609-74-7
• Molecular Weight: 298.467
• Mol File: 861609-74-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-chloro-6-iodo-4-nitroaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloro-6-iodo-4-nitroaniline(861609-74-7)
• EPA Substance Registry System: 2-chloro-6-iodo-4-nitroaniline(861609-74-7)

Safety Data

• Hazardous Substances Data: 861609-74-7(Hazardous Substances Data)

Upstream product

• 99-54-7 3,4-dichloronitrobenzene 
• 121-87-9 2-Chloro-4-nitroaniline 
• 861600-71-7 1-chloro-3-iodo-2,5-dinitro-benzene 
• 6293-83-0 2-iodo-4-nitrophenylamine 

Downstream Products

• 123158-76-9 1-chloro-3-iodo-5-nitrobenzene 
• 861547-81-1 1,2-dichloro-3-iodo-5-nitro-benzene 
• 83171-49-7 3-chloro-5-iodoaniline 
• 95-76-1 m,p-dichloroaniline 
• 684250-20-2 2-chloro-4-nitro-6-trimethylsilanylethynylaniline 

Relevant articles and documents

NCBSI/KI: A Reagent System for Iodination of Aromatics through in Situ Generation of I-Cl

In situ iodine monochloride (I-Cl) generation followed by iodination of aromatics using NCBSI/KI system has been developed. The NCBSI reagent requires no activation due to longer bond length, lower bond dissociation energy, and higher absolute charge density on nitrogen. The system is adequate for mono- and diiodination of a wide range of moderate to highly activated arenes with good yield and purity. Moreover, the precursor N-(benzenesulfonyl)benzenesulfonamide can be recovered and transformed to NCBSI, making the protocol eco-friendly and cost-effective.