3878-69-1

Basic information

• Product Name: 1-methyl-2-(1-methylbenzoimidazol-2-yl)benzoimidazole
• CAS NO: 3878-69-1
• Molecular Formula: C₁₆H₁₄N₄
• Molecular Weight: 262.314
• Mol File: 3878-69-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 495.6°Cat760mmHg
• Flash Point: 253.5°C
• Density: 1.27g/cm³
• CAS DataBase Reference: 1-methyl-2-(1-methylbenzoimidazol-2-yl)benzoimidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-2-(1-methylbenzoimidazol-2-yl)benzoimidazole(3878-69-1)
• EPA Substance Registry System: 1-methyl-2-(1-methylbenzoimidazol-2-yl)benzoimidazole(3878-69-1)

Safety Data

• Hazardous Substances Data: 3878-69-1(Hazardous Substances Data)

Usage

Molecular Structure

1-methyl-2-(1-methylbenzoimidazol-2-yl)benzoimidazole consists of two benzimidazole rings connected by a methyl group.

Heterocyclic Aromatic Compound

It is a derivative of benzimidazole, which is a heterocyclic aromatic organic compound.

Potential Applications

The compound may have potential applications in pharmaceutical research due to its benzimidazole derivative nature.

Biological Activities

Benzimidazole derivatives have been studied for various biological activities, such as anticancer, antimicrobial, and antifungal properties.

Methyl and Benzimidazole Groups

The presence of these groups in the compound suggests that it may exhibit similar biological activities.

Potential Drug Candidate

The compound could be a potential candidate for drug development or therapeutic research.

Further Studies Needed

Additional studies and analysis are necessary to determine the specific properties and potential applications of 1-methyl-2-(1-methylbenzoimidazol-2-yl)benzoimidazole.

Upstream product

• 1632-83-3 1-Methylbenzimidazole 
• 4981-92-4 1-benzylbenzimidazole 
• 640-61-9 N-methyl-p-toluenesulfonylamide 
• 85510-65-2 1-methyl-2-(1-methyl-3-benzoyl-1,2-dihydro-2-benzimidazolyl)benzimidazole 
• 98-88-4 benzoyl chloride 
• 119-65-3 isoquinoline 
• 91-22-5 quinoline 

Relevant articles and documents

An efficient and convenient Cu(OAc)2/air mediated oxidative coupling of azoles via C-H activation

An efficient and convenient approach to construct C-C bonds at the 2-position of azoles via Cu(OAc)2/air mediated oxidative homo- and cross-coupling reaction was reported. The corresponding products were obtained in good to excellent yield.

The reaction of 1-ethoxycarbonyl-3-methylbenzimidazolium salts with electrogenerated and potassium superoxide

1-Ethoxycarbonyl-3-methylbenzimidazolium salts, which have two possible reactive sites toward superoxide, were allowed to react with KO2 and electrogenerated superoxide to give the ring-opened products and 1- methylbenzimidazoles. The former compounds were specific products for superoxide, and the product distributions were revealed to depend on the counter cation of superoxide.

HETEROARYLATION OF ORGANOMETALLIC DERIVATIVES OF AZOLES BY N-ACYLBENZOPYRIDINIUM SALTS

The dimerization products 1,1'-dimethyl-2,2'-bibenzimidazolyl and 2,2'-dibenzoyl-1,1',2,2'-tetrahydro-1,1'-biisoquinoline were isolated in the reaction of 1-methyl-2-imidazolyl- and 1-methyl-2-benzimidazolylmagnesium bromides with isoquinoline (quinoline) in the presence of benzoyl chloride together with the products from the heteroarylation of benzimidazole (imidazole).Their formation indicates the possibility of reaction by the SET mechanism.