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Tillmans’ reagent

Thiol compounds 252, 254 Thione compounds 252, 254 Thiosemicarbazides, N-aryl- 248 Thiourea 107, 246,254, 269, 337 -, derivatives 322, 323 Thorium cations 144 Threonine 246 Thymol 153, 197, 198 -, derivatives 288 Tigogenin 59, 195 -, acetate 63 Tigogenone 59,60 Tillmans reagent 256 Tin, cations 144,311,398 -, organic derivatives see Organotin compounds... [Pg.734]

Although such compounds as L-xt/(o-hexulosonic acid and D-arabino-hexulosonic acid might form a similar enediol arrangement, it has been proved that they are not oxidized in an acidic medium, either polaro-graphically or by the Tillmans reagent. However, in an alkaline medium, anodically oxidizable compounds are formed from these compounds to a small extent. [Pg.171]

Organic acids 100 mg 2,6-Dichloroindophenol sodium salt in 100 ml ethanol (Tillman reagent) heat at 100°C for 5 min Red-orange zones on violet background... [Pg.584]

Dichloroindophenol, sodium salt Tillman s reagent C,2HeCl2NNa02 620-45-1 290.078 dkgrn cry sH20,Et0H, ace... [Pg.307]

Tillman s reagent 3200 1,1,1-Trichloro-tert-butyl alcohol 10258 2-one, (11 ) 1710... [Pg.717]

See other pages where Tillmans’ reagent is mentioned: [Pg.256]    [Pg.443]    [Pg.137]    [Pg.724]    [Pg.178]    [Pg.203]    [Pg.320]    [Pg.178]    [Pg.128]    [Pg.100]    [Pg.137]    [Pg.230]    [Pg.170]    [Pg.214]    [Pg.214]    [Pg.256]    [Pg.443]    [Pg.137]    [Pg.724]    [Pg.178]    [Pg.203]    [Pg.320]    [Pg.178]    [Pg.128]    [Pg.100]    [Pg.137]    [Pg.230]    [Pg.170]    [Pg.214]    [Pg.214]    [Pg.307]    [Pg.310]    [Pg.307]    [Pg.39]    [Pg.42]    [Pg.307]    [Pg.310]    [Pg.483]    [Pg.284]   
See also in sourсe #XX -- [ Pg.256 ]

See also in sourсe #XX -- [ Pg.177 ]

See also in sourсe #XX -- [ Pg.320 ]

See also in sourсe #XX -- [ Pg.178 ]



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