Aminoacridine hydrochloride

4-Aminobenzamidine Hydrochloride

A non-selective blocker of voltage-dependent K+-channels (Kv channels) that has greatest potency at Kv1 and Kv3 family members (IC₅₀s = 290, 590, 195, 13, 29, and 100 &microM for subunits 1.1, 1.

A non-selective blocker of voltage-dependent K+-channels (Kv channels) that has greatest potency at Kv1 and Kv3 family members (IC₅₀s = 290, 590, 195, 13, 29, and 100 &microM for subunits 1.1, 1.

A non-selective blocker of voltage-dependent K+-channels (Kv channels) that has greatest potency at Kv1 and Kv3 family members (IC₅₀s = 290, 590, 195, 13, 29, and 100 &microM for subunits 1.1, 1.

The consequences of one-electron oxidation and one-electron reduction were studied for 4-aminopyrimidine . Application 4-Aminopyrimidine has been used in the preparation of 1:4-dihydro-4-imino-1-methylpyrimidine hydriodide .

4-AMINOTHYMOL HYDROCHLORIDE

DescriptionAcylation reaction of 4-pyridylacetonitrile hydrochloride has been reported.4-Pyridylacetonitrile hydrochloride was used in preparation of (2Z)-3-(4-hydroxyphenyl)-4-pyridin-4-ylacrylonitrile.

5-Amino-2-chloropyridine undergoes Suzuki-Miyaura coupling with sterically hindered 2,6-dimethylphenylboronic acid . It undergoes facile temperature dependent displacement of chloride by bromide via Sandmeyer reaction to yield 2,5-dibromopyridine .

5-Amino-2-ethoxypyridine.

5-Amino-2-ethoxypyridine.

5-Amino-2-ethoxypyridine.

5-Aminomethyl-2-bromopyridine.