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

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

Downstream Products

• 622-50-4 4-Acetamido-1-iodobenzene 
• 157462-42-5 p-diacetoxyiodo-N-methylacetanilide 
• 60577-34-6 p-iodo-N-methylaniline 
• 612-03-3 4-(N-methylacetamido)toluene 
• 306768-12-7 (4-iodophenyl)-methyl-carbamic acid tert-butyl ester 

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

Visible-Light-Induced Decarboxylative Iodination of Aromatic Carboxylic Acids

A convenient, efficient and practical visible-light-induced decarboxylative iodination of aromatic carboxylic acids has been developed, and the corresponding aryl iodides were obtained in good yields. The method shows some advantages including the use of readily available aromatic carboxylic acids as the starting materials, simple and mild conditions, high efficiency, wide substrate scope and tolerance of various functional groups.

Highly Regioselective Iodination of N-Phenylureas with Iodine/Trichloroisocyanuric Acid

An efficient regioselective iodination of N-phenylureas was developed using iodine/trichloroisocyanuric acid in acetonitrile at room temperature. This protocol proved to be effective on a broad range of substituted N-phenylureas, forming the p-iodinated compounds in 65-96% yield under mild and neutral conditions.