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1H-Imidazole, 1-(4-methylphenyl)-2-(methylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116072-35-6

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116072-35-6 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 11 carbon (C) atoms, 12 hydrogen (H) atoms, 2 nitrogen (N) atoms, and 1 sulfur (S) atom.

Explanation

The compound is a derivative of the imidazole ring, which is a five-membered ring containing two nitrogen atoms. The presence of the imidazole ring gives the compound its unique chemical properties.

Explanation

The compound contains a 4-methylphenyl group (a phenyl ring with a methyl group attached to the 4th carbon) and a methylthio group (a sulfur atom bonded to a methyl group). These substituents contribute to the compound's reactivity and potential applications.

Explanation

The compound has been found to exhibit antifungal properties, which means it can inhibit the growth of fungi. Additionally, it has antioxidant properties, which means it can help protect cells from damage caused by reactive oxygen species.

Explanation

Due to its unique structure and biological activities, the compound is used as a starting material in the synthesis of various drugs and other bioactive compounds. It is also used in research to study the properties and potential applications of imidazole derivatives.

Explanation

The compound's structure, which includes a 4-methylphenyl group and a methylthio group, makes it a potential building block for the synthesis of various organic compounds. This can be useful in the development of new drugs, materials, or other chemical products.

Structure

1H-Imidazole derivative

Substituents

4-methylphenyl and methylthio groups

Biological Activities

Antifungal and antioxidant properties

Applications

Research and pharmaceutical synthesis

Potential Building Block

For the synthesis of organic compounds

Check Digit Verification of cas no

The CAS Registry Mumber 116072-35-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,0,7 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116072-35:
(8*1)+(7*1)+(6*6)+(5*0)+(4*7)+(3*2)+(2*3)+(1*5)=96
96 % 10 = 6
So 116072-35-6 is a valid CAS Registry Number.

116072-35-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methylphenyl)-2-methylsulfanylimidazole

1.2 Other means of identification

Product number -
Other names 2-methylsulfanyl-1-p-tolyl-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:116072-35-6 SDS

116072-35-6Downstream Products

116072-35-6Relevant academic research and scientific papers

Reaction of Dimethyl N-Aryl- and N-Alkylcarbonimidodithioates with Aminoacetaldehyde Diethyl Acetal: A Direct Synthesis of 1-Aryl- and 1-Alkyl-2-methylthioimidazoles

Pooranchand, Dinah,Ila, Hiriyakkanavar,Junjappa, Hiriyakkanavar

, p. 1136 - 1138 (2007/10/02)

The reaction of dimethyl N-aryl- or N-alkylcarbonimidodithioates with aminoacetaldehyde diethyl acetal in refluxing acetic acid affords 1-aryl or 1-alkyl-2-methylthioimidazoles in good yields.Dimethyl N-isopropylcarbonimidodithioate gave 1-isopropylimidazole-2(3H)-thione under similar conditions.

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