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109702-85-4

5-Nitro-2-(4-(5-nitro-1H-benzo[d]imidazol-2-yl)phenyl)-1H-benzo[d]imidazole is a complex organic compound with the molecular formula C18H10N6O4. It is characterized by the presence of two benzimidazole rings, each substituted with nitro groups and connected through a phenyl bridge. The compound exhibits a rich chemistry due to the presence of multiple nitro groups, which can participate in various chemical reactions such as reduction, substitution, and coupling. It is often used in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. The compound's properties, such as solubility and stability, can be influenced by the presence of these functional groups, making it a versatile building block in organic synthesis.

109702-85-4

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  • 5-NITRO-2-(4-(5-NITRO-1H-BENZO[D]IMIDAZOL-2-YL)PHENYL)-1H-BENZO[D]IMIDAZOLE

    Cas No: 109702-85-4

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  • 5-nitro-2-(4-(5-nitro-1H-benzo[d]imidazol-2-yl)phenyl)-1H-benzo[d]imidazole

    Cas No: 109702-85-4

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109702-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109702-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,7,0 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 109702-85:
(8*1)+(7*0)+(6*9)+(5*7)+(4*0)+(3*2)+(2*8)+(1*5)=124
124 % 10 = 4
So 109702-85-4 is a valid CAS Registry Number.

109702-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-nitro-2-[4-(6-nitro-1H-benzimidazol-2-yl)phenyl]-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 2,2'-phenylenebis(5-nitro-1H-benzimidazole)

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

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More Details:109702-85-4 SDS

109702-85-4Downstream Products

109702-85-4Relevant articles and documents

Mild and highly efficient method for the synthesis of 2-arylbenzimidazoles and 2-arylbenzothiazoles

Bahrami, Kiumars,Mehdi Khodaei,Naali, Fardin

, p. 6835 - 6837 (2008/12/22)

(Chemical Equation Presented) A new, convenient method for the syntheses of 2-substituted benzimidazole and benzothizole is described. Short reaction times, large-scale synthesis, easy and quick isolation of the products, excellent chemoselectivity, and excellent yields are the main advantages of this procedure.

A simple and efficient one-pot synthesis of 2-substituted benzimidazoles

Bahrami, Kiumars,Khodaei, Mohammad Mehdi,Kavianinia, Iman

, p. 547 - 550 (2008/01/03)

A simple and efficient procedure for the synthesis of substituted benzimidazoles through a one-pot condensation of o-phenylenediamines with aryl aldehydes in the presence of H2O2/HCl system in acetonitrile at room temperature is described. Short reaction time, large-scale synthesis, easy and quick isolation of the products, and excellent yields are the main advantages of this procedure. Georg Thieme Verlag Stuttgart.

H2O2/HCI as a new and efficient system for synthesis of 2-substituted benzimidazoles

Bahrami, Kiumars,Khodaei, Mohammad M.,Kavianinia, Iman

, p. 783 - 784 (2007/10/03)

The system, H2O2/HCI, oxidises carbon-nitrogen bonds for the synthesis of benzimidazoles from aldehydes and diamines in water at 100°C. Both aryl aldehydes bearing electron-donating and electron-withdrawing substituents afforded desired benzimidazoles in excellent yields. This procedure is also applicable to substituted o-phenylenediamines, which produced 2-phenylbenzimidazoles smoothly in excellent yields. The simplicity of the system, the use of water as the solvent, large-scale synthesis and easy work-up are main advantages of this procedure.

Synthesis of 2,5(6)-Disubstituted-benzimidazoles, 2-Substituted-5-(4-substituted-phenyl)-1,3,4-thiadiazoles and Imidazothioxanthene and Their Antifilarial Activity

Chauhan, P. M. S.,Bhakuni, D. S.

, p. 1146 - 1149 (2007/10/02)

2-Carbomethoxyaminothioxanthenoimidazol-12-one-13,13-dioxide (5), 2,5(6)-disubstituted-benzimidazoles (10-13) and 2-substituted-5-(3-nitro-4-substituted-phenyl)-1,3,4-thiadiazoles (18-24) have been synthesized and evaluated for their antifilarial a

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