1- ethyl pheny

Etbylpbenylcarbamate, Ethyl Ester or Ethyl-Pheny lure thane. (Athylphenylcarbamidsaure-... [Pg.193]

Rationalize tire major fragmentation pathways observed for ethyl pheny-lacetate A and diethyl phenylmalonate B... [Pg.393]

N,N-Bis -(2-hydroxy ethyl)-/ -pheny lene diamin e N,N-Bis -(2-hydroxyethyl)-/ -phenylene diamin e N,N-Bis -(2-hydroxyethyl)-/ -phenylene diamin e N,N-Bis -(2-hydroxyethyl)-/ -phenylene diamin e N,N-Bis -(2-hydroxy ethy l)-p-pheny len ediamin e N,N-Bis -(2-hydroxyethy 1)-p -phenylene diamin e 4-Amino-3-methylphenol 4-Amino-3-methylphenol 4-Amino-3-methylphenol 4-Amino-3-methylphenol 4-Amino-3-methylphenol 4-Amin o-3-methylp heno 1... [Pg.478]

C22H,0N2O 39666-27-8) see Isopropainide iodide a-12- bis( 1 -m cthy lethy l)amino]ethyl - - pheny Ibcnzene-acetonitrilc... [Pg.2310]

ChHmO 4-Ethyl- phenyl Dimethyl N,N-Dimethyl-4-ethyl- pheny ropiothioamidc 27... [Pg.106]

A suspension of 45 g 3-phenoxycarbonyloxy-1 -methyl-7-chloro-5-pheny -1,3-dihydro-2H-1,4-benzodiazepin-2-one in 450 ml methanol is treated with stirring, with 43 ml of a solution of dimethylamine in methanol (containlng31 gdimethylamine in 100 ml). Stirring ismaintained at 20°C to 25°C during 5 hours. The reaction mixture is filtered, and the filtrate is diluted with 450 ml water. The precipitate thus formed, is 3-(N,N-dimethylcarbamoyloxy)-1-methy -7-chloro-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one, which is collected on a filter, dried and recrystallized from ethyl acetate, and has a melting point of 173°C to 174°C. [Pg.221]

Certain of the monoalkylated ethyl phenylacetates have been further alkylated with alkyl and aralkyl halides to produce the corresponding disuhstituted phenylacetic esters.4 Ethyl 2-phenyl-propanoate has been alkylated by methyl iodide to give pure ethyl 2-methyl-2-pheny]propanoate in 81% yield. Similarly, the alkylations of ethyl 2-phenylhexanoate with methyl iodide, M-butyl bromide, and benzyl chloride gave the corresponding pure dialkylated products in 73%, 92%, and 72% yields, respectively. [Pg.74]

Glycine, JV-[A-[(pheny lmethoxylcarbonyl] -L phenylalanyl] -, ethyl ester [ 2778-34-9], 93... [Pg.134]

C H,4C1N0 54 2-34-2) see Tolazoline ethyl 2[Pg.2384]

Naphthol + N -ethyl-N (2-methanesulfon-amidoethyl)-2-methyl-l,4-pheny)enediamine (peroxide reagent)... [Pg.767]

Phenol, 2-6-di-tert-butyl-4-methyl 0 Phenol, 3-[2-(3-hydroxy-4 -methoxy-pheny 1 )-ethyl]-5-methoxy PI ... [Pg.37]

Phenol, 3-[2-(3-hydroxy-4 -methoxy-pheny 1 )-ethyl]-ethyl-5-methoxy 1 3172 Phenol, 3 - [2- (3 -iso-prenyl-4-hydroxy-5-methoxy-phenyl) -ethyl]-5-methoxy Pl 3172 Phenol, 3-[2-(4-hydroxy-phenyl)-ethyl]-5-methoxy 1 3172 Phenol, 4-vinyl Aer ... [Pg.37]

Depending on the substitution pattern and reaction conditions, 3-alkyl-4,5-dihydroisoxazoles aremetalated either at the 3a(exo)-position or at the C4(endo)-position18. Thus, metalation and alkylation of 4,5-dihydro-3-methyl-5-pheny]isoxazole (4) leads to both regioisomeric products, whereas endo deprotonation is more favorable in the case of the 3-ethyl derivative18. [Pg.1031]

Ethyl 2-Fluoro-2-nitrosooxy-3-oxo-3-phenyl- ElOa, 266 (11 -+ F) Ethyl 2-Fluoro-3-(4-nilro-pheny])-3-oxo- ElOa, 489 (H -> F)... [Pg.683]

Propanoate Ethyl 3-[2(or 3 or 4)-Bromo-pheny]]-3-fluoro-ElOa, 503 (OSiR3 F)... [Pg.683]

Heptenoate Ethyl 2-IV1 ethyI-4-pheny l thio-3-t rifluoi omethyl-tl0b2. 217... [Pg.721]

Malondioate Methyl [5-Mcthyl-2-(1-methyl-1-pheny l-etliy I)-cyclohcxyl] Ethyl-Ouoro- ElOa. 448 (H - E)... [Pg.729]

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