7025-33-4

Usage

Explanation

The compound consists of 15 carbon (C), 9 hydrogen (H), 1 bromine (Br), 2 nitrogen (N), and 1 sulfur (S) atoms.
2. Organic compound

Explanation

It is a compound containing carbon atoms bonded to hydrogen atoms and other elements.
3. Heterocyclic compound

Explanation

It contains a ring structure with more than one type of atom, such as nitrogen and sulfur, in the ring.
4. Benzimidazo thiazole ring system

Explanation

The compound has a fused ring structure consisting of a benzene ring attached to an imidazole ring, which in turn is connected to a thiazole ring.
5. Bromo-phenyl group attached

Explanation

A bromine atom is attached to a phenyl group (a benzene ring with one hydrogen atom replaced by a side chain), which is connected to the benzimidazo thiazole ring system.
6. Potential applications in medicinal chemistry

Explanation

Due to its unique structural features, the compound may be useful in the development of pharmaceuticals and agrochemicals.
7. Uses depending on specific application and research context

Explanation

The exact properties and uses of the compound may vary depending on the particular field of study and intended application.

Upstream product

• 136-95-8 2-amino-benzthiazole 
• 75-52-5 nitromethane 
• 1122-91-4 4-bromo-benzaldehyde 
• 99-90-1 para-bromoacetophenone 
• 98475-05-9 α-tosyloxy-4-bromoacetophenone 
• 99-73-0 para-bromophenacyl bromide 
• 99582-75-9 1-(4-Bromo-phenyl)-2-(2-imino-benzothiazol-3-yl)-ethanone; hydrobromide 
• 30192-89-3 1-(4-bromo-phenyl)-2-(2-imino-benzothiazol-3-yl)-ethanone 

Downstream Products

• 127204-72-2 2-(4-Bromo-phenyl)-benzo[d]imidazo[2,1-b]thiazole-3-carbaldehyde 
• 127204-60-8 3-[2-(4-Bromo-phenyl)-benzo[d]imidazo[2,1-b]thiazol-3-yl]-propionic acid 
• 127204-65-3 3-[2-(4-Bromo-phenyl)-benzo[d]imidazo[2,1-b]thiazol-3-yl]-propionic acid methyl ester 
• 127204-76-6 3-[2-(4-Bromo-phenyl)-benzo[d]imidazo[2,1-b]thiazol-3-yl]-3-hydroxy-propionic acid ethyl ester 
• 20138-75-4 2-(4-bromophenyl)-3-(thiocyanato)benzo[d]imidazo[2,1-b]thiazole 
• 1282523-75-4 2-(4'-methoxybiphenyl-4-yl)imidazo[2,1-b]benzothiazole 
• 121060-39-7 [2-(4-Bromo-phenyl)-benzo[d]imidazo[2,1-b]thiazol-3-ylmethyl]-trimethyl-ammonium; iodide 
• 121060-53-5 [2-(4-Bromo-phenyl)-benzo[d]imidazo[2,1-b]thiazol-3-yl]-acetic acid methyl ester 
• 121060-48-8 [2-(4-Bromo-phenyl)-benzo[d]imidazo[2,1-b]thiazol-3-yl]-acetic acid 
• 121060-46-6 2-(2-(4-bromophenyl)benzo[d]imidazo[2,1-b]thiazol-3-yl)acetamide 

Relevant academic research and scientific papers

Iron-catalyzed unprecedented formation of benzo[d]imidazo[2,1-b]thiazoles under solvent-free conditions

The unprecedented formation of benzo[d]imidazo[2,1-b]thiazole during iron-catalyzed coupling of 2-aminobenzothiazole, aldehydes with nitroalkane in air has been observed. This unique transformation possibly occurs through a sequential aza-Henry reaction and subsequent intramolecular cyclization, followed by denitration. A variety of substituted benzo[d]imidazo[2,1-b]thiazole are obtained using this protocol.

A convenient [hydroxy(tosyloxy)iodo]benzene-mediated one-pot synthesis of 2-arylimidazo[2,1-b[benzothiazoles

Several 2-arylimidazo[2,1-b]benzothiazoles (4) have been conveniently synthesized in one-pot reactions via α-tosyloxylation of enolizable ketones (1) using [hydroxy(tosyloxy)iodo]benzene 2 in acetonitrile, followed by treatment with 2-amino-6-(substituted

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).