102342-72-3

Basic information

• Product Name: 2,2'-dicarbomethoxyamino-5-5'-dibenzimidazolyl ketone
• Synonyms: 2,2'-dicarbomethoxyamino-5-5'-dibenzimidazolyl ketone
• CAS NO: 102342-72-3
• Molecular Formula: C19H16N6O5
• Molecular Weight: 408.36754
• Mol File: 102342-72-3.mol

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.584g/cm³
• CAS DataBase Reference: 2,2'-dicarbomethoxyamino-5-5'-dibenzimidazolyl ketone(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-dicarbomethoxyamino-5-5'-dibenzimidazolyl ketone(102342-72-3)
• EPA Substance Registry System: 2,2'-dicarbomethoxyamino-5-5'-dibenzimidazolyl ketone(102342-72-3)

Safety Data

• Hazardous Substances Data: 102342-72-3(Hazardous Substances Data)

Usage

Molecular structure

2,2'-dicarbomethoxyamino-5-5'-dibenzimidazolyl ketone has a complex molecular structure, which is a derivative of dibenzimidazole.

Functional groups

The compound contains carbomethoxyamino and ketone functional groups, which contribute to its unique properties and applications.

Use as a photoinitiator

It is commonly used in research and industry as a photoinitiator for light-cured materials, initiating the polymerization process when exposed to light.

UV absorber

The compound serves as a UV absorber in plastics and coatings, protecting products from sun damage by absorbing and converting ultraviolet radiation.

Potential medical applications

2,2'-dicarbomethoxyamino-5-5'-dibenzimidazolyl ketone has been studied for potential applications in medicine and other biological fields due to its unique structure and properties.

Safety precautions

The use of this chemical compound requires careful handling and proper safety precautions, as it may pose potential hazards if not used correctly.

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Relevant articles and documents

Studies in Potential Filaricides. 18. Synthesis of 2,2'-Disubstituted 5,5'-Dibenzimidazolyl Ketones and Related Compounds as Potential Anthelmintics

A series of 2,2'-disubstituted 5,5'-dibenzimidazolyl ketones (5-8) and related compounds (10-13) have benn synthesized of which 2,2'-bis(carbomethoxyamino>-5,5'-dibenzimidazolyl ketone (5) exhibited a broad spectrum of anthelmintic activity in experimental animals.At doses 10-50 mg/kg given intraperitoneally, 5 killed 100percent of the adult worms of Litomosoides carinii, Dipetalonema viteae, and Brugia malayi.By the oral route the macrofilaricidal efficacy of 5 was 97-100percent at 100-200 mg/kg * 5 days.The treated animals showed gradual disappearance of microfilariae and before autopsy thay became amicrofilariaemic.Some of the compounds (5, 10, 11) also showed 100percent efficacy against human hookworms and tapeworm, Ancylostoma ceylanicum in hamsters, and Hymenolepis nana in rats at a single oral dose of 50-250 mg/kg.Compound 5 was also effective against Syphacia obvelata in mice at a single oral dose of 100 mg/kg and was found to be well tolerated by mice up to an oral dose of 2500 mg/kg.

Synthesis and Anthelmintic Activity of Bisbenzimidazole-2-carbamates

The synthesis of bisbenzimidazole-2-carbamates (1-6) linked directly or by a one-atom bridge (CH2, CO, O, SO2, or S) at the 5 positions is described.Compound (4) shows interesting anthelmintic activity.