4-Amino-2-chloro-3-nitrophenol

Amino-5-nitro-4-chlorophenol. See 2-Amino-4-chloro-5-nitrophenol 2-Amino-3-nitrophenol CAS 603-85-0 EINECS/ELINCS 210-060-1 Synonyms 1 -Hydroxy-2-amino-3-nitrobenzene ... 

Oxidation base 13A. See 2-Chloro-p-phenylenediamine sulfate Oxidation base 16. See o-Phenylenediamine Oxidation base 19. See p-Aminoacetanilide Oxidation base 25. See 4-Amino-2-nitrophenol Oxidation base 33. See 1-Naphthol Oxidative base 12. See 4-Methoxy-m-phenylenediamine... 

Am i no-6-chloro-o-cresol 2-Am ino-3-hydroxypyridi ne 4-Am i no-2-hyd roxytol uene 2-Amino-3-nitrophenol 2-Amino-5-nitrophenol... 

Amino-2-nitrophenol o-Anisidine hydrochloride Bismuth citrate Black catechu (Acacia catechu) extract Chamomile Chamomile (Anthemis nobilis) oil 4-Chloro-o-phenylenediamine Chrysophanic acid Cobalt nitrate (ous) 2,4-Diaminoanisole sulfate tri hydrate... 

Following the classical syntheses of aromatic a-sialosides by phase transfer catalysis starting with the per-O-acetylated sialosyl chloride methyl ester, further aromatic a-sialosides could be prepared with sesamol (4), 2-chloro -nitrophenol (5), and 4-chloro-5-methyl-4-nitrophenol (6) [36]. In TcTS-sialylations none of these modified donor substrates showed any sialylation of methyl p-lactoside (7) to give the methyl sialyllactoside (8). It may be assumed that both steric and electronic factors affect interactions with aromatic and/or hydrophobic amino acid residues in the enzyme (Scheme 1). 

Aminophenol nitro derivatives 4-Amino-3-nitrophenol 3-Nitro-p-hydroethylaminophenol 2-Amino-3-nitrophenol HC Yellow No. 11 2-Amino-6-chloro-4-aminophenol l-Hydroxy-3-nitro-4-aminobenzene l-Hydroxy-3-nitro-4-j8-bydroxyethylaininobenzene l-Hydroxy-2-amino-3-nitrobenzene l-Hydroxy-2-j8-bydroxyethylamino-5-nitrobenzene l-Hydroxy-2-amino-4-nitro-6-chlorobenzene Orange Red Yellow-orange Yellow Red-orange... 

Acetamido-4-amino-6-chloro-s-triazine, see Atrazine Acetanilide, see Aniline, Chlorobenzene, Vinclozolin Acetic acid, see Acenaphthene, Acetaldehyde, Acetic anhydride. Acetone, Acetonitrile, Acrolein, Acrylonitrile, Aldicarb. Amyl acetate, sec-Amyl acetate, Bis(2-ethylhexyl) phthalate. Butyl acetate, sec-Butyl acetate, ferf-Butyl acetate, 2-Chlorophenol, Diazinon. 2,4-Dimethylphenol, 2,4-Dinitrophenol, 2,4-Dinitrotoluene, 1,4-Dioxane, 1,2-Diphenylhydrazine, Esfenvalerate. Ethyl acetate, Flucvthrinate. Formic acid, sec-Hexyl acetate. Isopropyl acetate, Isoamyl acetate. Isobutyl acetate, Methanol. Methyl acetate. 2-Methvl-2-butene. Methyl ferf-butvl ether. Methyl cellosolve acetate. 2-Methvlphenol. Methomvl. 4-Nitrophenol, Pentachlorophenol, Phenol. Propyl acetate. 1,1,1-Trichloroethane, Vinyl acetate. Vinyl chloride Acetoacetic acid, see Mevinphos Acetone, see Acrolein. Acrylonitrile. Atrazine. Butane. 

C6H4CIN03 4-chloro-2-nitrophenol 89-64-5 25.00 1.4818 2 6600 C6H4N4 2-amino-1 -propene-1,1,3-tricarbonitrile 868-54-2 25.00 1.3788 2... 

Catalytic hydrogenation of chloro-nitroaromatics is usually accompanied by dehalogenalion. However, the water-soluble complex prepared from [Pd(OAc)2] and TPPTS in DMSO-containing water reduced 5-chloro-2-nitrophenol to 2-amino-5-chlorophenol with high selectivity [231] (Scheme 3.25). 

Amino-4-chloro-5-nitrophenol CAS 6358-07-2 EINECS/ELINCS 228-760-0 Synonyms 2-Amino-5-nitro-4-chlorophenol Phenol, 2-amino-4-chloro-5-nitro-... 

Hydroxynitrobenzene. See o-Nitrophenol 4-Hydroxynitrobenzene p-Hydroxynitrobenzene. See p-Nitrophenol 4-Hydroxy-3-nitrobenzenearsonic acid. See 4-Hydroxy-3-nitrophenyl arsonic acid 2-Hydroxy-3-nitro-5-chloroaniline. See 2-Amino-4-chloro-6-nitrophenol... 

Acenaphthene 6-Acetoxy-2,4-dimethyl-m-dioxane Alkyl dimethyl ethylbenzyl ammonium chloride 2-Amino-4-chloro-6-nitrophenol Ammonium polysulfide Ammonium thiosulfate Anilazine Aniline Arsenic pentoxide Basic yellow 2 Bromoacenaphthylene 3-Bromochloro-5,5-dimethyl hydantoin p-Bromo-p-nitrostyrene Cadmium Cadmium chloride Calcium oxide Calcium polysulfide Carvacrol Cetalkonium chloride Cetethyidimonium bromide... 

Symmetrical carbonates are synthesized by carbonylation of the alcohols 4-chloro-tetrafluorophenol and 4-nitrophenol with phosgene. In this way, active esters of carbonic acids, such as di(p-chlorotetrafiuorophenyl) carbonate (di-Tfc-carbotMte) 875 [634] and di(p-nitrophenyl) carbonate (di-Dnp-carbonate) 717 [503], are produced. Di-Tfc-carbonate 875 is used to prepare p-chlorotetrajluorophenyl esters of N-protected amino acids and offers an advantageous alternative to pentafiuorophenyl esters, because pentafluorophenol is too stable in waste. 

Sandmeyer Reaction. The replacement of a diazonium group by halogen, nitrile, nitro, sulfhydryl, and other groups in the presence of a cuprous salt is known as the Sandmeyer reaction. An illustration of the use of this reaction is the preparation of 2-chloro-5-nitrophenol from the corresponding amino-phenol ... 

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