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1H-Benzimidazole,2-ethoxy-1-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1849-03-2

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1849-03-2 Usage

Structure

Benzimidazole derivative with an ethoxy and methyl substituent

Industrial applications

Building block in the synthesis of pharmaceuticals, pesticides, and other organic compounds; synthesis of heterocyclic compounds; reagent in chemical research

Biological activity

Potential as a pharmacologically active compound

Check Digit Verification of cas no

The CAS Registry Mumber 1849-03-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1849-03:
(6*1)+(5*8)+(4*4)+(3*9)+(2*0)+(1*3)=92
92 % 10 = 2
So 1849-03-2 is a valid CAS Registry Number.

1849-03-2SDS

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 2-Ethoxy-1-methyl-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 2-Aethoxy-1-methyl-benzimidazol

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:1849-03-2 SDS

1849-03-2Downstream Products

1849-03-2Relevant academic research and scientific papers

Cs2CO3-Promoted C?O Coupling Protocol Enables Solventless (Hetero)aryl Ether Synthesis under Air Atmosphere

Jiang, Bowen,Chen, Cheng,Fan, Guang-Gao,Sang, Wei,Cheng, Hua,Zhang, Rui,Yuan, Ye,Li, Qi-Zhong,Verpoort, Francis

, (2022/02/05)

In this work, a Cs2CO3-promoted synthetic approach was identified for (hetero)aryl ether synthesis via the C?O coupling of various (hetero)aryl chlorides and alcohols/phenol. To our delight, the reactions could be carried out under transition-metal-free and solvent-free conditions. Moreover, analytical-grade reagents and air atmosphere were readily tolerated. To showcase the practical usefulness of the present protocol, the assembly of a bioactive molecule was facilely realized and the gram-scale production of selected ether products was also efficiently accomplished. In addition, density functional theory (DFT) studies, along with a few mechanistic experiments, were conducted to elucidate a proposed reaction pathway and rationalize the pivotal role of Cs2CO3 in promoting this process. Hopefully, this work could provide useful information for researchers who are engaging in C?O cross-coupling reactions.

A facile one-pot synthesis of benzimidazoles from 2-nitroanilines by reductive cyclization

Liu, Zheng,Li, Haihong,Zhao, Qingjie,Shen, Jingshan

scheme or table, p. 1907 - 1911 (2009/04/06)

A facile one-pot process to prepare benzimidazole derivatives is described. Reductive cyclization of a serial of 2-nitroanilines with orthoesters in the presence of Pd/C in methanol at room temperature, which is promoted by a catalytic amount of acetic acid, affords the corresponding benzimidazole derivatives in high yields.

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