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2-(2-nitrobenzyl)-1H-benzo[d]imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71443-44-2

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71443-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71443-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,4 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71443-44:
(7*7)+(6*1)+(5*4)+(4*4)+(3*3)+(2*4)+(1*4)=112
112 % 10 = 2
So 71443-44-2 is a valid CAS Registry Number.

71443-44-2Downstream Products

71443-44-2Relevant academic research and scientific papers

Microwave-Assisted Synthesis of Benzimidazole-Linked Indoline and Indole Hybrids from C-2 Linked (o-Aminobenzyl)benzimidazoles

Lee, Yun-Ta,Chiu, Feng-Yu,Barve, Indrajeet J.,Sun, Chung-Ming

, p. 502 - 512 (2018)

An efficient and novel synthesis of benzimidazole-linked indoline hybrids via an unconventional Pictet-Spengler-type condensation of C-2 linked (o-aminobenzyl)benzimidazoles with aldehydes and ketones under microwave irradiation has been explored. The key

Diverting Reactive Intermediates Toward Unusual Chemistry: Unexpected Anthranil Products from Davis-Beirut Reaction

Zhu, Jie S.,Son, Jung-Ho,Teuthorn, Andrew P.,Haddadin, Makhluf J.,Kurth, Mark J.,Tantillo, Dean J.

, p. 10875 - 10882 (2017)

The discovery of a new variation on the Davis-Beirut reaction is described in which an atypical heterocyclic framework (the anthranil or benzo[c]isoxazole framework) is formed as the result of diversion of a key reactive intermediate away from its expected reactivity - a potentially general approach to reaction design and development. Experimental and computational support for the proposed mechanism and origins of altered reactivity are described.

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