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102342-72-3

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102342-72-3 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.

Check Digit Verification of cas no

The CAS Registry Mumber 102342-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,3,4 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102342-72:
(8*1)+(7*0)+(6*2)+(5*3)+(4*4)+(3*2)+(2*7)+(1*2)=73
73 % 10 = 3
So 102342-72-3 is a valid CAS Registry Number.

102342-72-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl N-[6-[2-(methoxycarbonylamino)-3H-benzimidazole-5-carbonyl]-1H-benzimidazol-2-yl]carbamate

1.2 Other means of identification

Product number -
Other names Carbamic acid,(carbonylbis(1H-benzimidazole-5,2-diyl))bis-,dimethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:102342-72-3 SDS

102342-72-3Downstream Products

102342-72-3Relevant articles and documents

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

Abuzar, Syed,Sharma, Satyavan,Fatma, Nigar,Gupta, S.,Murthy, P. K.,et al.

, p. 1296 - 1299 (1986)

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.

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