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4-ethyl-1H-imidazole is a heterocyclic organic compound characterized by a five-membered ring structure composed of three carbon atoms, two nitrogen atoms, and an ethyl group attached to one of the carbons. This versatile compound is utilized in various fields due to its unique chemical properties and potential applications.

19141-85-6

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19141-85-6 Usage

Uses

Used in Pharmaceutical Industry:
4-ethyl-1H-imidazole serves as a building block for the development of pharmaceuticals, contributing to the creation of new drugs and therapeutic agents. Its unique structure allows it to form stable complexes with various biological targets, enhancing the efficacy and selectivity of the resulting medications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-ethyl-1H-imidazole is employed as a key component in the synthesis of pesticides and other crop protection agents. Its ability to form stable complexes with target organisms helps improve the effectiveness and safety of these products.
Used as an Antimicrobial Agent:
4-ethyl-1H-imidazole has been identified as a potential antimicrobial agent, exhibiting activity against pathogenic fungi and bacteria. Its ability to disrupt microbial growth and survival makes it a promising candidate for the development of new antimicrobial treatments and preventive measures.
Used in Coordination Chemistry:
As a ligand in coordination chemistry, 4-ethyl-1H-imidazole plays a crucial role in the formation of metal complexes. These complexes have potential applications in various fields, including catalysis, materials science, and environmental remediation, due to their unique electronic and structural properties.
Used as a Catalyst in Organic Synthesis:
4-ethyl-1H-imidazole has been investigated for its potential use as a catalyst in organic synthesis. Its ability to facilitate various chemical reactions, such as cyclization, condensation, and rearrangement, makes it a valuable tool in the development of new synthetic pathways and the production of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 19141-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,4 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19141-85:
(7*1)+(6*9)+(5*1)+(4*4)+(3*1)+(2*8)+(1*5)=106
106 % 10 = 6
So 19141-85-6 is a valid CAS Registry Number.

19141-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Ethyl-1H-imidazole

1.2 Other means of identification

Product number -
Other names 4-ethyl-1H-imidazole

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:19141-85-6 SDS

19141-85-6Relevant academic research and scientific papers

Synthesis of 4,5-substituted imidazoles by a fast condensation of 1,2-diketones and urotropine in heterogeneous medium

Bratulescu, George

, p. 2319 - 2320 (2009)

Starting from 1,2-diketones and urotropine in the presence of ammonium acetate, a simple and efficient solventless microwave-assisted synthesis of 4,5-disubstituted imidazoles was accomplished. Georg Thieme Verlag Stuttgart.

COMPOUDS AND USES THEREOF IN MODULATING AMYLOID BETA

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Paragraph 0172; 0174, (2015/11/16)

Novel compounds, compositions, and kits are provided. Methods of modulating Aβ levels, and methods of treating a disease associated with aberrant Aβ levels are also provided.

Novel farnesyl protein transferase inhibitors as antitumor agents

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Page 204, (2010/02/07)

Disclosed are novel tricyclic compounds represented by the formula (1.0): and a pharmaceutically acceptable salt or solvate thereof. The compounds are useful for inhibiting farnesyl protein transferase. Also disclosed are pharmaceutical compositions comprising compounds of formula 1.0. Also disclosed are methods of treating cancer using the compounds of formula 1.0.

A Two-Step Synthesis of Imidazoles from Aldehydes via 4-Tosyloxazolines

Horne, David A.,Yakushijin, Kenichi,Buechi, George

, p. 139 - 154 (2007/10/02)

Imidazoles with substituents in the 4- and 4,5-positions were prepared by heating 4-tosyloxazolines in saturated methanolic ammonia.Similar treatment of these oxazolines with monoalkylamines regioselectively affords 1,4-disubstituted imidazoles.When oxazolines bearing an ethyl group at the 4-position were heated with alkylamines, however, a regioisomeric mixture of di- or trisubstituted imidazoles was produced.These reactions proceed via an intermolecular condensation of α-amino ketones and amidines or intramolecular cyclization of α-amidino ketone intermediates, respectively.

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