Antipsychotics

4-Phenylthiazole.

4-Phenylthiazole.

Application 4-Piperidone monohydrate hydrochloride was used in the generation of compound libraries based on sub-reactions of an Ugi multicomponent reaction (MCR) .

Application 4-Piperidone monohydrate hydrochloride was used in the generation of compound libraries based on sub-reactions of an Ugi multicomponent reaction (MCR) .

4-Quinolinol (4-quinolone) is a quinolone compound which forms the core moiety of antibacterials such as norfloxacin, nalidixic acid, ciprofloxacin and cinoxacin.

4-Quinolinol (4-quinolone) is a quinolone compound which forms the core moiety of antibacterials such as norfloxacin, nalidixic acid, ciprofloxacin and cinoxacin.

4-Quinolinol (4-quinolone) is a quinolone compound which forms the core moiety of antibacterials such as norfloxacin, nalidixic acid, ciprofloxacin and cinoxacin.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

4- tert -Butylcatechol, in the presence of O 2 catalyzed by tyrosinase, yields 4- tert -butyl- o -benzoquinone . Electrochemical oxidation of 4- tert -butylcatechol in the presence of 4-hydroxycoumarin as nucleophile has been studied using cyclic

4- tert -Butylcatechol, in the presence of O 2 catalyzed by tyrosinase, yields 4- tert -butyl- o -benzoquinone . Electrochemical oxidation of 4- tert -butylcatechol in the presence of 4-hydroxycoumarin as nucleophile has been studied using cyclic

4- tert -Butylcatechol,in the presence of O 2 catalyzed by tyrosinase, yields 4- tert -butyl- o -benzoquinone . Electrochemical oxidation of 4- tert -Butylcatechol in the presence of 4-hydroxycoumarin as nucleophile has been studied using cyclic

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Melting range (lower value): &#8805 52 &#176C Melting range (upper value): &#8804 57 &#176C Identity (IR): passes test