Welcome to LookChem.com Sign In|Join Free

CAS

  • or

26286-51-1

Post Buying Request

26286-51-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

26286-51-1 Usage

Description

2-methyl-1-(2-nitrophenyl)imidazole is a chemical compound with the molecular formula C10H9N3O2. It is a derivative of imidazole and contains a methyl group and a nitrophenyl group. 2-methyl-1-(2-nitrophenyl)imidazole is known for its potential biological and medicinal properties, as well as its applications in the synthesis of pharmaceuticals and agrochemicals.

Uses

Used in Pharmaceutical Industry:
2-methyl-1-(2-nitrophenyl)imidazole is used as a building block for the synthesis of pharmaceuticals due to its potential biological and medicinal properties. Its unique structure allows it to be a valuable component in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, 2-methyl-1-(2-nitrophenyl)imidazole is utilized as a building block for the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Material Science:
2-methyl-1-(2-nitrophenyl)imidazole is also investigated for its potential use in the development of new materials, thanks to its chemical properties and structural characteristics.
Used in Coordination Chemistry:
As a potential ligand, 2-methyl-1-(2-nitrophenyl)imidazole is explored in coordination chemistry for its ability to form complexes with metal ions, which can lead to advances in various chemical and material applications.
Used in Antimicrobial and Anti-Fungal Applications:
2-methyl-1-(2-nitrophenyl)imidazole has been studied for its antimicrobial and antifungal activities, making it a candidate for use in applications that require the inhibition of microbial growth, such as in medical or environmental settings.

Check Digit Verification of cas no

The CAS Registry Mumber 26286-51-1 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 26286-51:
(7*2)+(6*6)+(5*2)+(4*8)+(3*6)+(2*5)+(1*1)=121
121 % 10 = 1
So 26286-51-1 is a valid CAS Registry Number.

26286-51-1SDS

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-Methyl-1-(2-nitrophenyl)-1H-imidazole

1.2 Other means of identification

Product number -
Other names isopropyl 2-naphthyl ketone

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:26286-51-1 SDS

26286-51-1Relevant 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

Novel compounds possessing potent cAMP and cGMP phosphodiesterase inhibitory activity. Synthesis and cardiovascular effects of a series of imidazo[1,2-a]quinoxalinones and imidazo[1,5-a]quinoxalinones and their aza analogues

Davey,Erhardt,Cantor,Greenberg,Ingebretsen,Wiggins

, p. 2671 - 2677 (2007/10/02)

A series of novel imidazoquinoxalinones and their aza analogues were prepared by the cyclization of o-amino(1H-imidazol-1-yl)aryls and heteroaryls with carbonyldiimidazole. The compounds were screened for inhibition of Type I and Type IV phosphodiesterase

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 26286-51-1