1365756-96-2

Usage

Heterocyclic compound

The compound has a complex structure that includes a benzoimidazole ring, a phenyl group, and a 5-bromopyridine moiety.

Structure

The structure consists of a benzo[d]imidazole ring fused to a phenyl group and a 5-bromopyridine moiety.

Medicinal chemistry use

It is often used as a building block for the synthesis of various bioactive molecules and pharmaceuticals.

Reactivity

The presence of the bromine and pyridine functional groups imparts specific reactivity to the compound.

Properties

The compound has unique properties due to its aromatic structure and potential for diverse chemical modifications.

Valuable scaffold

It serves as a valuable scaffold for the design of novel compounds with targeted biological activities.

Application in new drugs and agrochemicals

The compound is useful for the development of new drugs and agrochemicals because of its reactivity and properties.

Upstream product

• 534-85-0 N-phenyl-1,2-benzenediamine 
• 137178-88-2 5-bromopyridine-2-carbonyl chloride 

Downstream Products

• 1613149-50-0 N-phenyl-N-(4-(5-(6-(1-phenyl-1H-benzo[d]imidazol-2-yl)pyridin-3-yl)pyrazin-2-yl)phenyl)naphthalen-1-amine 
• 1613149-48-6 N,N-diphenyl-4-(5-(6-(1-phenyl-1H-benzo[d]imidazol-2-yl)pyridin-3-yl)pyrazin-2-yl)aniline 
• 1572938-37-4 1-phenyl-2-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)-1H-benzo[d]imidazole 

Relevant academic research and scientific papers

Organic light emitting host materials

Polyphenylene compounds such as compounds represented by Formulas 1-28 may be used in electronic devices such as organic light-emitting devices. For example, the compounds may be used as host material in an emissive layer.

SUBSTITUTED BIPYRIDINES FOR USE IN ORGANIC LIGHT-EMITTING DEVICES

Optionally substituted bipyridine compounds, optionally substituted phenylbipyridine compounds, or optionally substituted bis-phenylbipyridine compounds may be useful in light-emitting devices. Some examples include, but are not limited to, optionally substituted 4-(5-(6-(4-(diphenylamino)phenyl)pyridin-3-yl)pyridin-2-yl)-N,N- diphenylbenzenamine, optionally substituted 9-(4-(5-(6-(4-(9H-carbazol-9- yl)phenyl)pyridin-3-yl)pyridin-2-yl)phenyl)-9H-carbazole, optionally substituted 4-(5-(6- (benzo[d]thiazol-2-yl)pyridin-3-yl)pyridin-2-yl)-N,N-diphenylbenzenamine, optionally substituted 4-(5-(6-(benzo[d]oxazol-2-yl)pyridin-3-yl)pyridin-2-yl)-N,N- diphenylbenzenamine, optionally substituted N,N-diphenyl-4-(5-(6-(l -phenyl- 1H- benzo[d]imidazol-2-yl)pyridin-3-yl)pyridin-2-yl)benzenamine, optionally substitut-ed 4- (5-(6-(4-(9H-carbazol-9-yl)phenyl)pyridin-3-yl)pyridin-2-yl)-N,N-diphenylbenzenamine, optionally substituted 2-(5-(6-(benzo[d]thiazol-2-yl)pyridin-3-yl)pyridin-2- yl)benzo[d]thiazole, optionally substituted 2-(5-(6-(benzo[d]thiazol-2-yl)pyridin-3- yl)pyridin-2-yl)benzo[d]oxazole, optionally substituted 9-(4-(5-(6-( benzo[d]thiazol-2- yl)pyridin-3-yl)pyridin-2-yl)phenyl)-9H-carbazole, optionally substituted 9-(4-(5-(6- (benzo[d]oxazol-2-yl)pyridin-3-yl)pyridin-2-yl)phenyl)-9H-carbazole, optionally substituted 9-(4-(6'-(l-phenyl-lH-benzo[d]imidazol-2-yl)-3,3'-bipyridin-6-yl)phenyl)-9H- carbazole, and 6,6'-bis(9-phenyl-9H-carbazol-3-yl)-3,3'-bipyridine.