51279-01-7

Basic information

• Product Name: Acetamide, N-(3-ethylphenyl)-
• CAS NO: 51279-01-7
• Molecular Formula: C10H13NO
• Molecular Weight: 163.219
• Mol File: 51279-01-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Acetamide, N-(3-ethylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N-(3-ethylphenyl)-(51279-01-7)
• EPA Substance Registry System: Acetamide, N-(3-ethylphenyl)-(51279-01-7)

Safety Data

• Hazardous Substances Data: 51279-01-7(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 587-02-0 m-ethylaniline 
• 108-05-4 vinyl acetate 
• 122-79-2 Phenyl acetate 
• 108-22-5 Isopropenyl acetate 
• 2161-86-6 2,4-diacetylphloroglucinol 
• 105-45-3 acetoacetic acid methyl ester 
• 7664-93-9 sulfuric acid 
• 103030-63-3 1-(3-ethyl-phenyl)-ethanone oxime 
• 99-03-6 1-(3-aminophenyl)ethanone 

Downstream Products

• 863973-55-1 N-(5-ethyl-2-nitrophenyl)acetamide 
• 1416258-99-5 N-(5-ethyl-2-(2-hydroxy-1,3-dioxo-2,3-dihydro-1H-inden-2-yl)phenyl)acetamide 
• 1282610-46-1 3-acetamido-6-nitro-ethylbenzol 
• 1364188-17-9 N-(2-ethyl-2',4',6'-trimethylbiphenyl-4-yl)-N-mesitylacetamide 
• 926216-99-1 4-acetamido-2-ethylbenzene-1-sulfonyl chloride 
• 1308254-71-8 4-amino-2-ethyl-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)benzenesulfonamide 
• 1331892-96-6 N-(3-ethyl-4-(N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)sulfamoyl)phenyl)acetamide 
• 174753-27-6 C₄₇H₅₁N₃Si 
• 174753-29-8 C₄₄H₄₃N₃ 
• 174753-28-7 (2-Ethyl-4-{2-ethyl-4-[2-ethyl-4-(2-ethyl-4-iodo-phenylethynyl)-phenylethynyl]-phenylethynyl}-phenylethynyl)-trimethyl-silane 
• 174753-24-3 C₂₇H₃₅N₃Si 
• 174753-26-5 C₂₄H₂₇N₃ 
• 174753-25-4 [2-Ethyl-4-(2-ethyl-4-iodo-phenylethynyl)-phenylethynyl]-trimethyl-silane 
• 174753-16-3 1-(diethyltriazenyl)-3-ethyl-4-<(trimethylsilyl)ethynyl>benzene 

Relevant articles and documents

Promiscuous activity of C-acyltransferase from: Pseudomonas protegens: Synthesis of acetanilides in aqueous buffer

Amide bond formation has considerable significance in synthetic chemistry. Although the C-acyltransferase from Pseudomonas protegens has been found to catalyze C-C bond formation in nature as well as in in vitro experiments with non-natural substrates, it is now shown that the enzyme is also able to catalyze amide formation using aniline derivatives as substrates with promiscuous activity. Importantly, the amide formation was enabled in aqueous buffer. Identifying phenyl acetate as the most suitable acetyl donor, the products were obtained with up to >99% conversion and up to 99% isolated yield.

Palladium-catalyzed C-H bond acylation of acetanilides with benzylic alcohols under aqueous conditions

Palladium-catalyzed dehydrogenative coupling reactions between acetanilides and benzylic alcohols under aqueous conditions are reported. A wide range of benzophenone derivatives could be obtained in good to excellent yields up to 98 %. Mechanism studies showed that a bimetallic palladium cyclopalladated complex might be involved in the catalysis.

BORON-CONTAINING SMALL MOLECULES

This invention relates to 6-substituted benzoxaborole compounds of the following formula and their use for treating bacterial infections.