Anthelmintic benzene derivatives

Aminoacetaldehyde dimethyl acetal reacts with sulfone, followed by hydrolysis and reductive amination by adding desired piperazine derivative to yield piperazine derivatives of 2-furanyl[1,2,4]triazolo[1,5-a][1,3,5]triazine. Aminoacetaldehyde

Aminoacetaldehyde dimethyl acetal reacts with sulfone, followed by hydrolysis and reductive amination by adding desired piperazine derivative to yield piperazine derivatives of 2-furanyl[1,2,4]triazolo[1,5-a][1,3,5]triazine. Aminoacetaldehyde

Aminoacetaldehyde dimethyl acetal reacts with sulfone, followed by hydrolysis and reductive amination by adding desired piperazine derivative to yield piperazine derivatives of 2-furanyl[1,2,4]triazolo[1,5-a][1,3,5]triazine. Aminoacetaldehyde

Anthra[9，1，2-cde]benzo[rst]pentaphene-5，10-dione.

Anthra[9，1，2-cde]benzo[rst]pentaphene-5，10-dione.

Anthra[9，1，2-cde]benzo[rst]pentaphene-5，10-dione.

Anthra[9，1，2-cde]benzo[rst]pentaphene-5，10-dione.

Anthraquinone-D8.

Anthraquinone-D8.

Azidobenzene is an aromatic azide generally used in copper(I)-catalyzed azide-alkyne cycloaddition reactions. Azidobenzene solution can undergo click reaction with alkyne-functionalized oligomers to form O -ester-functionalized o-phenylenes, a

DescriptionAzidobenzene solution can undergo click reaction with alkyne-functionalized oligomers to formO-ester-functionalized o-phenylenes, a group of aromatic foldamers with a good folding tendency in most solvents.Azidobenzene is an aromatic

DescriptionAzidobenzene solution can undergo click reaction with alkyne-functionalized oligomers to formO-ester-functionalized o-phenylenes, a group of aromatic foldamers with a good folding tendency in most solvents.Azidobenzene is an aromatic