V- acetamide

Acetamide, V-[ 2-(6-a cetyl-1,3 -benzodioxol-5-yl)ethyll-[61426-48-01,7 ACETAMIDE, N- [ 2-(2-ACETYL-4,5-DI-METHOXYPHENYL)ETIIYL] -[57621-03-1], 3... 

Acetamides, (V-arylalkyl-, 56, 7 5- 2-Acetamidoethyl)-6-acetyl 1,3-benzo-dioxole, 56, 7... 

The behavior of two substituted organic acetamides (.V.iV-diethyl- and /V,/V-dipropyl-) were studied by ESR techniques. The spectra were characteristic of free radicals involving H-atom loss from the N-alkyl groups (297). 

Chemical Name /V,/V-dimethyldiphenyl acetamide V,/V-dimethyl-a-phenyl-benzeneacetamide... 

Tretyakov and Filimonov (219) describe a coordinative interaction between benzonitrile and aprotic sites on magnesium oxide, and Zecchina et al. (256) came to the same conclusion for the adsorption of propionitrile, benzonitrile, and acrylonitrile on a chromia-silica catalyst. Chapman and Hair (257) observed an additional chemical transformation of benzonitrile on alumina-containing surfaces, which they describe as an oxidation. Knozinger and Krietenbrink (255) have shown that acetonitrile is hydrolyzed on alumina by basic OH- ions, even at temperatures below 100°C. This reaction may be described as shown in Scheme 2. The surface acetamide (V) is subsequently transformed into a surface acetate at higher temperatures. Additional reactions on alumina are a dissociative adsorption and polymerizations (255) analogous to those observed for hydrogen cyanide by Low and Ramamurthy (258), and a dissociative adsorption. Thus, acetonitrile must certainly be refused as a probe molecule and specific poison. 

There are generally two types of drug emulsions, those in which the drug j.s already dmo/tW in the oil pluise before production (this is de.seribed as parenteral nutrition, usually with the aid of organic solvents such as ethanol or dintethyl acetamide v/torr/v before appliceition. However, with the... 

A/-[4-(Aminosulfonyl)phenyl]acetamide 5-Amino-1,3,4-thiadiazole-2(3/ -thione 2-Amino-4(5A)-thiazolone A/-(Aminothioxomethyl)acetamide /V-Amino-2-thioxo-4-thiazolidinone 1-Amino-2.2.2-trichloroethanol... 

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