Phenylmercuric nitrate

Application 4-Nitro-o-phenylenediamine was used to study the in vitro activation of 4-nitro-o-phenylenediamine into a potent mutagen in Salmonella typhimurium strain TA98 . Biochem/physiol Actions 4-Nitro-o-phenylenediamine is a direct-acting

Application 4-Nitro-o-phenylenediamine was used to study the in vitro activation of 4-nitro-o-phenylenediamine into a potent mutagen in Salmonella typhimurium strain TA98 . Biochem/physiol Actions 4-Nitro-o-phenylenediamine is a direct-acting

A chromogenic substrate for endoglucanases and cellobiohydrolases.

A chromogenic substrate for endoglucanases and cellobiohydrolases.

4-Phenyl-1-butanol is oxidized by ceric ammonium nitrate in acetonitrile to afford 2-phenyltetrahydrofuran . It undergoes cyclization in presence of phosphoric acid at high temperature to yield tetralin .

4-Phenyl-1-butanol is oxidized by ceric ammonium nitrate in acetonitrile to afford 2-phenyltetrahydrofuran . It undergoes cyclization in presence of phosphoric acid at high temperature to yield tetralin .

4-Phenyl-1-buten-4-ol

C₆H₅CH₂CH₂CH=CH₂ CAS#: 768-56-9 F.W.: 132.21

C₆H₅CH₂CH₂CH=CH₂ CAS#: 768-56-9 F.W.: 132.21

4-Phenyl-2-butanol undergoes (&#951 5 -pentaphenylcyclopentadienyl)RuCl(CO) 2 catalyzed racemization efficiently at room temperature in the presence of a base . 4-Phenyl-2-butanol on reaction with sulfuric acid yields polymer .

trans - 4-Phenyl-3-buten-2-one is substrate for glutathione transferase . It reacts with methyl- and benzylguanidine to yield aromatic N 2 -substituted 2-pyrimidinamines .

Application 4-Phenylbenzylamine may be used in the synthesis of: squaric acid asymmetric diamides of glycopeptide antibiotics asymmetric diamides of daunomycin and carminomycin N