99582-73-7

Upstream product

• 136-95-8 2-amino-benzthiazole 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 

Downstream Products

• 121060-41-1 [2-(4-Methoxy-phenyl)-benzo[d]imidazo[2,1-b]thiazol-3-ylmethyl]-trimethyl-ammonium; iodide 
• 121060-55-7 methyl [2-(4-methoxyphenyl)imidazo[2,1-b][1,3]benzothiazol-3-yl]acetate 
• 121076-29-7 [2-(4-Methoxy-phenyl)-benzo[d]imidazo[2,1-b]thiazol-3-ylmethyl]-dimethyl-amine 
• 121060-50-2 [2-(4-Methoxy-phenyl)-benzo[d]imidazo[2,1-b]thiazol-3-yl]-acetic acid 
• 121060-44-4 [2-(4-Methoxy-phenyl)-benzo[d]imidazo[2,1-b]thiazol-3-yl]-acetonitrile 
• 116923-26-3 2-(2-Imino-benzothiazol-3-yl)-1-(4-methoxy-phenyl)-ethanol 
• 26921-83-5 2-(4-methoxyphenyl)benzo[d]imidazo[2,1-b]thiazole 

Relevant academic research and scientific papers

DIHYDRO-5,6 IMIDAZOTHIAZOLES, DIHYDRO-2,3 IMIDAZOBENZOTHIAZOLES, ANALOGUES DU LEVAMISOLE

New compounds containing 5,6-dihydro imidazothiazole 2,3,5,6-tetrahydro imidazothiazole and 2,3-dihydro imidazobenzothiazole rings, substituted by heterocycles analogue to chromones, were synthesized and screened against three nematodes, in vitro.The results indicate moderate anthelmintic properties, compared to levamisole; nevertheless, some products exhibit a significant degree of activity.

Imidazobenzothiazoles. 2. New Immunosuppressive Agents

A series of 2-phenylimidazobenzothiazole derivatives was prepared and tested for immunological activities.Some of the compounds showed significant suppressive activity of delayed type hypersensitivity (DTH) without inhibition of humoral immunity in mice by oral administration.The most active compound was 2-(m-hydroxyphenyl)imidazobenzothiazole (20).