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26286-55-5

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26286-55-5 Usage

General Description

2-(2-Methyl-1H-imidazol-1-yl)aniline is a chemical compound with the molecular formula C10H12N2. It is an aniline derivative with a substituted imidazolyl group. 2-(2-Methyl-1H-imidazol-1-yl)aniline is commonly used in organic synthesis as a building block for various pharmaceuticals and agrochemicals. It has also been studied for its potential biological and pharmacological activities, including its antitumor and antimicrobial properties. Additionally, 2-(2-Methyl-1H-imidazol-1-yl)aniline has been investigated for its potential use in dye chemistry and as a corrosion inhibitor in metal coatings. Overall, this compound possesses diverse potential applications in both the chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 26286-55-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,8 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26286-55:
(7*2)+(6*6)+(5*2)+(4*8)+(3*6)+(2*5)+(1*5)=125
125 % 10 = 5
So 26286-55-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3/c1-8-12-6-7-13(8)10-5-3-2-4-9(10)11/h2-7H,11H2,1H3

26286-55-5SDS

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-methylimidazol-1-yl)aniline

1.2 Other means of identification

Product number -
Other names 1-o-Aminophenyl-2-methylimidazol

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:26286-55-5 SDS

26286-55-5Downstream Products

26286-55-5Relevant articles and documents

Imidazo[1,2-a]pyrazine, Imidazo[1,5-a]quinoxaline and?Pyrazolo[1,5-a]quinoxaline derivatives as IKK1 and IKK2 inhibitors

Patinote, Cindy,Bou Karroum, Nour,Moarbess, Georges,Deleuze-Masquefa, Carine,Hadj-Kaddour, Kamel,Cuq, Pierre,Diab-Assaf, Mona,Kassab, Issam,Bonnet, Pierre-Antoine

, p. 909 - 919 (2017/07/27)

The transcription nuclear factor NF-κB plays a pivotal role in chronic and acute inflammatory diseases. Among the several and diverse strategies for inhibiting NF-κB, one of the most effective approach considered by the pharmaceutical industry seems to be

In vitro and in vivo anti-tumoral activities of imidazo[1,2-a]quinoxaline, imidazo[1,5-a]quinoxaline, and pyrazolo[1,5-a]quinoxaline derivatives

Moarbess, Georges,Deleuze-Masquefa, Carine,Bonnard, Vanessa,Gayraud-Paniagua, Stephanie,Vidal, Jean-Remi,Bressolle, Francoise,Pinguet, Frederic,Bonnet, Pierre-Antoine

, p. 6601 - 6610 (2008/12/22)

Imidazoquinoxaline and pyrazoloquinoxaline derivatives, analogues of imiquimod, were synthesized, and their in vitro cytotoxic and pharmacodynamic activities were evaluated. In vitro cytotoxicity studies were assessed against melanoma (A375, M4Be, RPMI-75

Efficient ligand-mediated ullmann coupling of anilnies and azoles

-

, (2008/06/13)

The present invention provides of method of preparing phenyl-substituted azoles. This method uses an efficient ligand-accelerated Ullmann coupling reaction of anilines with azoles. The coupling products are useful for preparing factor Xa inhibitors.

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