Anaesthetic drugs & related adjuncts & analeptics

Reaction of 4-bromoaniline with acetic acid and potassium thiocynate in solution of bromine in acetic acid yields 2-amino-6-bromobenzothiazole. 2-Amino-6-bromobenzothiazole can also be synthesized from 2-aminobenzothiazole via monobromination with

Reaction of 4-bromoaniline with acetic acid and potassium thiocynate in solution of bromine in acetic acid yields 2-amino-6-bromobenzothiazole. 2-Amino-6-bromobenzothiazole can also be synthesized from 2-aminobenzothiazole via monobromination with

2-Amino-6-ethoxybenzothiazole

2-Amino-6-hydroxybenzothiazole

The anti-tetanus activity of 2-amino-6-methylbenzothiazole, a muscle relactant, was studied . Application 2-Amino-6-methylbenzothiazole was used in the preparation of 2-[(6-methyl-1,3-benzothiazol-2-yl)amino]- N -[2-(substituted

Voltammetric behavior of 2-amino-6-nitrobenzothiazole has been investigated using direct current voltammetry and differential pulse voltammetry . Application 2-Amino-6-nitrobenzothiazole has been used: as model analyte for voltammetric

Voltammetric behavior of 2-amino-6-nitrobenzothiazole has been investigated using direct current voltammetry and differential pulse voltammetry . Application 2-Amino-6-nitrobenzothiazole has been used: as model analyte for voltammetric

Application 2-Aminobenzimidazole was used in the hydrolysis of a choline carbonate . It was also used in the synthesis of imidazo[1,2-a]benzimidazoles .

Application 2-Aminobenzimidazole was used in the hydrolysis of a choline carbonate . It was also used in the synthesis of imidazo[1,2-a]benzimidazoles .

2-Aminobenzothiazole is a neutral carrier (ionophore) used to construct a poly (vinyl chloride)-based membrane electrode for determination of Ce 3+ ions . 2-Aminobenzothiazole bonds chemically to multiwalled carbon nanotubes to produce a sorbent

2-Aminobenzothiazole is a neutral carrier (ionophore) used to construct a poly (vinyl chloride)-based membrane electrode for determination of Ce 3+ ions . 2-Aminobenzothiazole bonds chemically to multiwalled carbon nanotubes to produce a sorbent

Analysis Note Assay (HClO&#8324): &#8805 98.0 % Melting range (lower value): &#8805 127 &#176C Melting range (upper value): &#8804 130 &#176C Identity (IR): passes test