58010-65-4

Basic information

• Product Name: Benzamide, N-benzoyl-4-methyl-
• CAS NO: 58010-65-4
• Molecular Formula: C15H13NO2
• Molecular Weight: 239.274
• Mol File: 58010-65-4.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Benzamide, N-benzoyl-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-benzoyl-4-methyl-(58010-65-4)
• EPA Substance Registry System: Benzamide, N-benzoyl-4-methyl-(58010-65-4)

Safety Data

• Hazardous Substances Data: 58010-65-4(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 619-55-6 para-methylbenzamide 
• 98-07-7 Benzotrichlorid 
• 874-60-2 4-methyl-benzoyl chloride 
• 71-43-2 benzene 
• 7647-01-0 hydrogenchloride 
• 201230-82-2 carbon monoxide 
• 624-31-7 4-tolyl iodide 
• 55-21-0 benzamide 
• 591-50-4 iodobenzene 
• 26177-45-7 4-methylbenzylamine hydrochloride 
• 100-52-7 benzaldehyde 
• 589-18-4 4-Methylbenzyl alcohol 
• 3287-99-8 benzylamine hydrochloride 

Relevant articles and documents

Traceless selenocarboxylates for the one-pot synthesis of amides and derivatives

We have recently reported a one-pot procedure for glycosyl amides synthesis using selenocarboxylate as traceless reagent. Herein, we present a further application of selenocarboxylate-azide reaction for amide bond formation on a broader range of substrates, including heterocyclic systems and fatty acid. This method proved to be highly efficient for the synthesis of primary and secondary amides, sulfonamides, imides, phosphoramide and also carbamate.

Copper-catalyzed synthesis of imides from aldehydes or alcohols and amine hydrochloride salts

An efficient approach to imides has been developed. With tert-butyl hydroperoxide (TBHP) as the oxidant, CuBr (20 mol-%) as the catalyst, and PhI(OAc)2 (50 mol-%) as the additive, aldehydes or alcohols reacted with amine hydrochloride salts to provide imides in moderate to good yields. A possible reaction pathway for the formation of the products is also discussed in this paper.

Palladium-catalyzed aminocarbonylation of aryl iodides with amides and N-alkyl anilines

A novel and efficient palladium-catalyzed aminocarbonylation of aryl iodides with amides and N-alkyl anilines has been developed. The reaction tolerates a wide range of functional groups and is a reliable method for the rapid synthesis of a variety of valuable imides and tertiary benzanilides under an atmospheric pressure of CO. Copyright