1438400-28-2

Basic information

• Product Name: N-(2-acetyl-5-methoxyphenyl)-4-methylbenzenesulfonamide
• Synonyms: N-(2-acetyl-5-methoxyphenyl)-4-methylbenzenesulfonamide
• CAS NO: 1438400-28-2
• Molecular Weight: 319.381
• Mol File: 1438400-28-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(2-acetyl-5-methoxyphenyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-acetyl-5-methoxyphenyl)-4-methylbenzenesulfonamide(1438400-28-2)
• EPA Substance Registry System: N-(2-acetyl-5-methoxyphenyl)-4-methylbenzenesulfonamide(1438400-28-2)

Safety Data

• Hazardous Substances Data: 1438400-28-2(Hazardous Substances Data)

Upstream product

• 42465-53-2 1-(2-amino-4-methoxyphenyl)ethanone 
• 98-59-9 p-toluenesulfonyl chloride 
• 941-55-9 4-toluenesulfonyl azide 
• 3609-53-8 methyl 4-acetylbenzoate 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 99-90-1 para-bromoacetophenone 

Downstream Products

• 42465-53-2 1-(2-amino-4-methoxyphenyl)ethanone 

Relevant articles and documents

A Palladium- and Copper-Catalyzed Synthesis of Dihydro[1,2-b]indenoindole-9-ol and Benzofuro[3,2-b]indolines: Metal-Controlled Intramolecular C-C and C-O Bond-Forming Reactions

A palladium- and copper-catalyzed synthesis of dihydro[1,2-b]indenoindole-9-ol and benzofuro[3,2-b]indolines has been developed, whereby the same starting material is employed for the synthesis of both heterocyclic scaffolds and the selectivity of the pro

Ru(ii)-catalyzed intermolecular ortho-C-H amidation of aromatic ketones with sulfonyl azides

Ru(ii)-catalyzed intermolecular ortho-C-H amidation of weakly coordinating aromatic ketones with sulfonyl azides is reported. The developed reaction protocol can be extended to various substituted aromatic ketones to afford a wide range of desired C-N bond formation products in good yields.

Ru(ii)-catalyzed intermolecular C-H amidation of weakly coordinating ketones

An efficient Ru(ii)-catalyzed intermolecular amidation of weakly coordinating ketones with sulfonyl azides via C-H bond activation is described. The reaction proceeds with high functional group tolerance, providing a novel approach to practical ketone-directed intermolecular C-N bond formation in the absence of an additional oxidant.