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4-Nitrophenyl N-phenyl

THE USE OF POLYSTYRYLSULFONYL CHLORIDE RESIN AS A SOLID SUPPORTED CONDENSATION REAGENT FOR THE FORMATION OF ESTERS SYNTHESIS OF N-[(9-FLUORENYLMETHOXY)CARBONYL]-L-ASPARTIC ACID a tert-BUTYL ESTER, P (2-ETHYL[(lE)-(4-NITROPHENYL)AZO] PHENYL]AMINO]ETHYL ESTER... [Pg.124]

To a 50-mL polypropylene vial (Note 1) are added 0.839 g (2.67 mmol) of 2-[ethyl[4-[(lE)-(4-nitrophenyl)azo]phenyl]amino]ethanol (Disperse Red 1, Note 2), 0.985 g of (2.39 mmol) N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-aspartic acid,l-(l, 1-dimethylethyl) ester (Fmoc-L-Asp-OtBu, Note 3), 3.26 g (4.73 mmol) of polystyrylsulfonyl chloride resin (Note 4), and 30 mL anhydrous methylene chloride (Note 5). The vial is capped and the mixture is shaken for five min (Note 6). N-Methylimidazole (0.764 mL, 9.58 mmol) is then added to the deep red mixture (Note 7) and the resulting mixture is shaken for 2 hr (Note 8). [Pg.124]

Chemical Name 1-Piperazinecarbothioamide, 4-methyl-N-(4-((4-nitrophenyl) amino)phenyl)-... [Pg.290]

Fluoro-l-phenylpyrazole-4-carboxamides 304 have been formed by condensation of the 5-fluoro-l-phenylpyrazole-4-carboxylic acid 303 with amines (Equation 58) <2000EJ0823>. 4-Benzoyl-l-(4-nitrophenyl)-5-phenyl-l//-pyrazole-3-carboxylic acid 305 was converted via reactions of its acid chloride with alcohols or N-nucleophiles, into the corresponding ester or amide derivatives 306 (Equation 59) <2004CHE1039>. Resin-bound pyrazole-4-carboxylic... [Pg.51]

N-acetyl-4 (or S)-(2-(S-nitro-2-furanyI)ethenyl]-4-acetyI-1 (2-nitrophenyl)-3-phenyl-4-acetyl-1 -(4-nitrophenyl)-5-phenyl-4-[4-(acefyloxy)-2-hydroxybenzoyl]-5-methyl-2-phenyl-1 -acetyl-4-( 1,3-pentadienyl)-S-propyl-... [Pg.145]

Nitrophenyl-diazenyl) phenyl-l,3-diamine, 467 N-(4-Nitrophenyl)-l-prolinol, 46 Octadecylacrylate, 537... [Pg.591]

Synthesis of N,N,-bis(4-nitrophenyl)-N, N -bis[4-(2-phenyl-2-isopropyl) phenyl]- ,4-phenylene-diamine (3). In a 250 ml three neck round-bottom lisk was placed bis- [4-(2-pheiiyl- 2-isopropyl)phenyl]-4-aminopheitylamine (2) (7.26 g, 14.63 mmol), 4-Qtoro-nitro- benzene (4.13 g, 29.27 mmol), cesium Qioride (4.41 g, 29.27 mmol), and 80 ml DMSO. The mixture was heated with stirring at 120"C for 24 hr. The reaction mixture was cooled and then poured into 500 ml methanol. The red precipitate was collected by titration and dried under vacuum. The product was puriffed by sihca gel colunrn chromatography ( -hexane dichloromethane = 1 1) to afford dinitio compoimd (3) in a 65% yield mp 224-225 "C (by DSC 10°C /min). [Pg.11]

Synonyms Ammonium, (2-(p-((2-chloro-4-nitrophenyl) azo) phenethylamino) ethyl) trimethyl- Cl 11085 Ethanaminium, 2-((4-((2-chloro-4-nitrophenyl) azo) phenyl) ethylamino)-N,N,N-trimethyl Red GTL Empiricai C19H2SCINSO2 Properties M.w. 390.94 Toxicoiogy Mutagen TSCA listed Uses Dye for polyacrylonitrile Manuf./Distrib. Aakash Chems. Dyestuffs http //members.aoi.com/aakashchem/informati on.htmi] Aashiana Dyestuffs http //www.aashianadyestuffs.com] Albanil Dyestuff Int l. http //www.aibaniidye.com] D G Dyes Leadertech Colors Org. Dyestuffs http //www.organicdye.com]... [Pg.397]

Ethanaminium, 2-((4-((2-chloro-4-nitrophenyl) azo) phenyl) ethylamino)-N,N,N-trimethyl. See Basic red 18... [Pg.1662]

Nitrophenyl)-3-phenyl-5-( 1 -phthalazinyl)formazan, N-00143 6-Bromo-1,2-naphthoquinone Dioxime, in B-00538... [Pg.1218]

Hydrazides are formed by the acylation of hydrazines, and have a C-N bond of rather low chemical stability toward hydrolysis. It is, therefore, not surprising that the cleavage of this bond represents a major metabolic pathway for most hydrazides. The reaction is catalyzed by amidases since it can be inhibited by O-ethyl 0-(4-nitrophenyl) phenyl phosphothionate or bis(4-nitrophenyl) phosphate, which are classical inhibitors of this enzyme. [Pg.165]

N-(4-nitrophenyl)-amino acids N-(2,4-dinitrophenyl)-amino acids 8) and 3-nitro-2-pyridyl amino acids have been of considerable interest. A generally applicable mechanistic scheme does not exist so far, and except for 3-nitrophenyl acetate in ortho and/or -para position of the phenyl (pyridyl) ring seems to be a prerequisite for efficient decarboxylation. [Pg.81]


See other pages where 4-Nitrophenyl N-phenyl is mentioned: [Pg.110]    [Pg.38]    [Pg.168]    [Pg.168]    [Pg.168]    [Pg.257]    [Pg.110]    [Pg.38]    [Pg.168]    [Pg.168]    [Pg.168]    [Pg.257]    [Pg.74]    [Pg.31]    [Pg.528]    [Pg.74]    [Pg.177]    [Pg.438]    [Pg.81]    [Pg.380]    [Pg.380]    [Pg.396]    [Pg.396]    [Pg.396]    [Pg.74]    [Pg.74]    [Pg.529]    [Pg.52]    [Pg.919]    [Pg.55]    [Pg.82]    [Pg.739]    [Pg.1008]    [Pg.1137]    [Pg.1335]    [Pg.225]    [Pg.323]    [Pg.1266]    [Pg.144]   
See also in sourсe #XX -- [ Pg.528 ]




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4-Nitrophenyl phenyl

N- -2-phenyl

N-Phenylation

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