62404-59-5

Basic information

• Product Name: N-(4-iodophenyl)-N-methylacetamide
• Synonyms: N-(4-iodophenyl)-N-methylacetamide
• CAS NO: 62404-59-5
• Molecular Formula: C₉H₁₀INO
• Molecular Weight: 275.08627
• Mol File: 62404-59-5.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(4-iodophenyl)-N-methylacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-iodophenyl)-N-methylacetamide(62404-59-5)
• EPA Substance Registry System: N-(4-iodophenyl)-N-methylacetamide(62404-59-5)

Safety Data

• Hazardous Substances Data: 62404-59-5(Hazardous Substances Data)

Upstream product

• 579-10-2 N-acetyl-N-methylaniline 
• 157462-42-5 p-diacetoxyiodo-N-methylacetanilide 
• 622-50-4 4-Acetamido-1-iodobenzene 
• 74-88-4 methyl iodide 
• 100-61-8 N-methylaniline 
• 26961-99-9 4-(N-acetyl-N-methylamino)benzoic acid 
• 60577-34-6 p-iodo-N-methylaniline 
• 108-24-7 acetic anhydride 
• 540-37-4 p-aminoiodobenzene 

Downstream Products

• 157462-42-5 p-diacetoxyiodo-N-methylacetanilide 
• 171285-77-1 N-methyl-4'-<<4-(2,2,4-trimethyl-1,3-dioxolan-4-yl)thien-2-yl>thio>acetanilide 
• 852926-65-9 N-(4-diphenylphosphanyl-phenyl)-N-methyl-acetamide 
• 622-50-4 4-Acetamido-1-iodobenzene 
• 60577-34-6 p-iodo-N-methylaniline 
• 306768-12-7 (4-iodophenyl)-methyl-carbamic acid tert-butyl ester 
• 612-03-3 4-(N-methylacetamido)toluene 

Relevant articles and documents

Cobalt-Catalyzed Hydroalkynylation of Vinylaziridines

Transition metal-catalyzed hydroalkynylation reactions are efficient transformations allowing the straightforward formation of functionalized alkynes. Therein, we disclose the cobalt-catalyzed hydroalkynylation of vinylaziridines giving rise to both linea

Formamide as an Unconventional Amine Protecting Group for PET Radiochemistry

We developed a versatile, rapid, and robust high-yielding radiochemistry-adapted protocol utilizing formamides as masking groups for secondary and tertiary amines. Selective reducing conditions were devised using borane reagents. In this protocol formamid

Thermolysis and radiofluorination of diaryliodonium salts derived from anilines

Aniline-derived diaryliodonium salts were synthesized and functionalized in good to excellent yields by judicious utilization of electron-withdrawing protecting groups. This simple approach opens another route to radiolabeling amino arenes in relatively complex molecules, such as flutemetamol.