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P-Aminophenyl disulfide

The author s group tried to find the S MIE in the direct photolysis of is p-aminophenyl disulfide (ArS-SAr) in SDS micelles at room temperature [8]. [Pg.134]

In the preparation of di(p-aminophenyl) disulfide, sodium sulfide first displaces the activated halogen atom and then reduces the nitro group. The terminal step is... [Pg.1286]

A mixture of p-chloronitrobenzene, Na2S, and water slowly heated to boiling with rapid agitation, refluxed 20 hrs., cooled to ca. 15 , filtered, the filtrate concentrated, and treated dropwise at 65-70° with 30% H202 over a period of ca. 2 hrs. p-aminophenyl disulfide. Y 58-64%. (C. C. Price and Gr. W. Stacy, Org. Synth. 28, 14 (1948).)... [Pg.173]

Aminophenyl disulfide Cystine, 2-Nitrophenyl disulfide Methyl disulfide, p-tolyl disulfide Benzyl disulfide Naphthothiophenes (NTH)... [Pg.79]

An industrial process for the preparation of 2-p-aminophenyl-6-methylbenzothiazole (562) (dehydrothiotoluidine) is based on the high temperature reaction of sulfur with p-toluidine (561 Scheme 297). A similar process involves the simultaneous action of sulfur and carbon disulfide on a primary arylamine. BenzothiazoIe-2-thione (564) (2-mercaptobenzothiazoIe) is synthesized industrially by reaction of aniline (563) with sulfur and carbon disulfide (Scheme 298). In this synthesis, sulfur plays the role of a dehydrogenating reagent and may be replaced by nitrobenzene. [Pg.326]

BIS(2-AMINOPHENYL)DISULFIDE see DXJ800 BIS(o-AMINOPHENYL)DISULFIDE see DXJ800 l,l -BIS(2-AMINOPHENYL)DISULFIDE see DXJ800 BIS(4-AMINOPHENYL)ETHER see OPMOOO BIS(p-AMINOPHENYL)ETHER see OPMOOO BIS(4-AMINOPHENYL)METHANE see MJQOOO BIS(p-AMINOPHENYL)METHANE see MJQOOO 2, 4-BIS(AMINOPHENYL)METHANE see MJP750 BIS(4-AMINOPHENYL) SULFIDE see TFIOOO BIS(p-AMINOPHENYL)SULFIDE see TFIOOO BIS(4-AMINOPHENYL) SULFONE see SOA500... [Pg.1539]

C12H12N2S, Di-(p-aminophen.yl) sulfide 97 C12H12N2S2, Di (o-aminophenyl) disulfide. 97... [Pg.311]

Holzmann250 has described the reaction of W,JV-dialkylanilines with sulfur chlorides, which gives sulfides and disulfides. In the presence of lead oxide, aniline and sulfur afford bis-(p-aminophenyl) sulfide as follows 251... [Pg.632]

Kim and coworkers have reported a synthetic route to diverse heterocyclic compounds through the nucleophihc addition of P-amino carbonyl compounds 79 to 3-halo-4-methoxybenzynes 78 (Scheme 12.25) [51]. The benzyne intermediate 78 was generated from 5-(3-halo-4-methoxyphenyl)thianthrenium perchlorates 77 upon treatment with lithium diisopropylamide (LDA) in THF at reflux. P-Amino carbonyl compounds, such as P-amino ketones, esters, amides and aldehydes, all react smoothly with benzyne 78 under the reported reaction conditions. Moreover, bis(2-aminophenyl) disulfide, 2-aminophenyl benzenesulfonate... [Pg.423]

Tomb RR, Lepoittevin J-P, Caussade P (1991) Contact allergy to 2-aminophenyl disulfide. Contact Dermatitis 25 196-197... [Pg.885]


See other pages where P-Aminophenyl disulfide is mentioned: [Pg.877]    [Pg.133]    [Pg.851]    [Pg.239]    [Pg.340]    [Pg.8]    [Pg.2716]    [Pg.106]    [Pg.133]    [Pg.340]    [Pg.877]    [Pg.133]    [Pg.851]    [Pg.239]    [Pg.340]    [Pg.8]    [Pg.2716]    [Pg.106]    [Pg.133]    [Pg.340]    [Pg.512]    [Pg.462]    [Pg.107]    [Pg.107]    [Pg.45]    [Pg.352]   
See also in sourсe #XX -- [ Pg.14 , Pg.28 ]




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