57056-93-6

Basic information

• Product Name: Benzenamine, 2-iodo-N-methyl-
• CAS NO: 57056-93-6
• Molecular Formula: C7H8IN
• Molecular Weight: 233.052
• Mol File: 57056-93-6.mol
• Article Data: 45

Chemical Properties

• CAS DataBase Reference: Benzenamine, 2-iodo-N-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 2-iodo-N-methyl-(57056-93-6)
• EPA Substance Registry System: Benzenamine, 2-iodo-N-methyl-(57056-93-6)

Safety Data

• Hazardous Substances Data: 57056-93-6(Hazardous Substances Data)

Upstream product

• 615-43-0 2-iodophenylamine 
• 77-78-1 dimethyl sulfate 
• 10113-39-0 N-formyl-2-iodoaniline 
• 172984-02-0 N-(2-iodoanilinomethyl)succinimide 
• 390432-51-6 2-{[N-(2-iodophenyl)-N-methylamino]methyl}cyclohexanone 
• 900537-30-6 N-(2-iodophenyl)-N-methyl-4-nitrobenzenesulfonamide 
• 68-11-1 mercaptoacetic acid 
• 74-88-4 methyl iodide 
• 296273-08-0 N-(2-iodophenyl)-4-nitrobenzenesulfonamide 
• 109-63-7 trifluoroborane diethyl ether 
• 100-61-8 N-methylaniline 
• 50-00-0 formaldehyd 
• 1221594-10-0 N-tert-butoxycarbonyl-2-iodo-N-methylaniline 
• 917-54-4 methyllithium 

Downstream Products

• 107365-60-6 2-iodo-N-methyl-N-trimethylsilylaniline 
• 135190-49-7 N-(2-Iodophenyl)-N-methylpropanamide 
• 90585-26-5 N-(2-iodophenyl)-N-methylacetamide 
• 150982-95-9 N-(2-Iodophenyl)-N,3-dimethylbutanamide 
• 57056-89-0 N-(but-3-en-1-yl)-2-iodo-N-methylaniline 
• 57056-87-8 o-(N-allyl-N-methylamino)iodobenzene 
• 172983-99-2 2-[(2-Iodo-phenyl)-methyl-amino]-1-(4-trifluoromethyl-phenyl)-ethanone 
• 172983-95-8 2-[(2-Iodo-phenyl)-methyl-amino]-1-(3-methoxy-phenyl)-ethanone 
• 172983-93-6 2-[(2-Iodo-phenyl)-methyl-amino]-1-phenyl-ethanone 
• 172983-97-0 1-(4-Chloro-phenyl)-2-[(2-iodo-phenyl)-methyl-amino]-ethanone 
• 172983-98-1 1-(4-Bromo-phenyl)-2-[(2-iodo-phenyl)-methyl-amino]-ethanone 
• 172983-96-9 1-(4-Fluoro-phenyl)-2-[(2-iodo-phenyl)-methyl-amino]-ethanone 
• 172984-00-8 1-[(2-Iodo-phenyl)-methyl-amino]-propan-2-one 
• 172983-94-7 2-[(2-Iodo-phenyl)-methyl-amino]-1-(4-methoxy-phenyl)-ethanone 

Relevant articles and documents

Accessing Unsymmetrically Linked Heterocycles through Stereoselective Palladium-Catalyzed Domino Cyclization

A palladium-catalyzed strategy is presented to synthesize unsymmetrically linked heterocycles within stereoselective tetrasubstituted olefins. This reaction is proposed to occur via a vinyl-PdII intermediate capable of initiating the cyclizatio

Catalytic and Enantioselective Control of the C–N Stereogenic Axis via the Pictet–Spengler Reaction

An unprecedented example of a chiral phosphoric acid-catalyzed atroposelective Pictet–Spengler reaction of N-arylindoles is reported. Highly enantioenriched N-aryl-tetrahydro-β-carbolines with C?N bond axial chirality are obtained via dynamic kinetic reso

One-Pot, Three-Step Synthesis of Benzoxazinones via Use of the Bpin Group as a Masked Nucleophile

The utilization of the Bpin group as a pronucleophile to facilitate the assembly of cyclic carbamates has been achieved. This one-pot process involves an initial copper-catalyzed borylation, a subsequent C-B bond oxidation to generate the reactive alcohol