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2-(2-METHOXY-PHENYL)-1H-IMIDAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52091-35-7

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52091-35-7 Usage

Imidazole ring

Five-membered ring with two nitrogen atoms
The compound features an imidazole ring, which is a five-membered ring structure containing two nitrogen atoms and three carbon atoms. This ring is known for its stability and is a common structural motif in many biologically active compounds.

Methoxy group attached to the phenyl ring

-OCH3
A methoxy group (-OCH3) is attached to the phenyl ring in the compound, which is a type of ether functional group consisting of an oxygen atom bonded to a methyl group (-CH3). This substitution can influence the compound's properties, such as solubility, reactivity, and biological activity.
5. Potential pharmaceutical applications
Due to its unique structure, 2-(2-Methoxy-phenyl)-1H-imidazole may have potential applications in the pharmaceutical industry. Its specific biological activities and potential benefits are not yet fully understood and require further research and development.
6. Need for further research
Although the compound has potential pharmaceutical applications, more research is needed to determine its specific uses, benefits, and any possible side effects or toxicity. This will help in understanding its true potential and possible therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 52091-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,9 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52091-35:
(7*5)+(6*2)+(5*0)+(4*9)+(3*1)+(2*3)+(1*5)=97
97 % 10 = 7
So 52091-35-7 is a valid CAS Registry Number.

52091-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methoxyphenyl)-1H-imidazole

1.2 Other means of identification

Product number -
Other names 2-(2-methoxy-phenyl)-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:52091-35-7 SDS

52091-35-7Downstream Products

52091-35-7Relevant academic research and scientific papers

Study of synthesis of 2-(2-alkoxyphenyl)-1h-imidazoles. Comparison of oxidative aromatization reactions of imidazolines

Parik, Patrik,Senauerova, Sylva,Liskova, Vlasta,Handlir, Karel,Ludwig, Miroslav

, p. 835 - 841 (2007/10/03)

The reaction of methyl salicylate with ethane-1,2-diamine has been used to prepare 2-(2-hydroxyphenyl)-1H-imidazoline. This compound was alkylated with alkyl halides to give five new 2-(2-alkoxyphenyl)-1H-imidazolines (alkyl = propyl, isopropyl, isobutyl,

2,5-DIAZACYCLOPENTADIENYLIDENE: A STANDARD CARBENE OR A HIGHLY REACTIVE DIRADICAL?

Bru, Nuria,Vilarrasa, Jaume

, p. 1489 - 1492 (2007/10/02)

2,5-Diazacyclopentadienylidene (2H-imidazolidene), generated either by photolysis or thermolysis from 2-diazo-2H-imidazole, reacts with benzene derivatives to give mainly a mixture of o-, m-, p-substitued 2-phenylimidazoles.The carbene shows a strong diradical character, in sharp contrast with the well-known behavior of cyclopentadienylidene.

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