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25364-43-6

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25364-43-6 Usage

General Description

1-(M-TOLYL)IMIDAZOLE, also known as 1-(3-methylphenyl)-1H-imidazole, is a chemical compound from the group of imidazoles known for their therapeutic uses in pharmaceuticals, particularly in antifungal drugs. Its molecular formula is C10H10N2, with a molecular weight of 158.2 g/mol. 1-(M-TOLYL)IMIDAZOLE possesses properties of both the imidazole and toluene ring, which are aromatic and primarily composed of carbon and hydrogen atoms, which makes it a versatile component in chemical reactions. However, information about this specific compound's reactivity, toxicity, and potential hazards is fairly limited, suggesting additional research is required for a comprehensive understanding of its properties and uses.

Check Digit Verification of cas no

The CAS Registry Mumber 25364-43-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,6 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25364-43:
(7*2)+(6*5)+(5*3)+(4*6)+(3*4)+(2*4)+(1*3)=106
106 % 10 = 6
So 25364-43-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2/c1-9-3-2-4-10(7-9)12-6-5-11-8-12/h2-8H,1H3

25364-43-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(m-Tolyl)imidazole

1.2 Other means of identification

Product number -
Other names 1-(3-methylphenyl)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:25364-43-6 SDS

25364-43-6Relevant articles and documents

Heterogeneous catalyzed aryl-nitrogen bond formations using a valine derivative bridged metal-organic coordination polymer

Wu, Chuan-De,Li, Li,Shi, Lian-Xu

, p. 6790 - 6794 (2009)

A new 1D macrocyclic copper(ii) coordination polymer, [CuL2] (1, L = N-(4-pyridyl)-d,l-valine), based on a valine derived ligand was synthesized and characterized by single-crystal X-ray diffraction studies. The catalytic experiments showed tha

A Pd/Cu-Free magnetic cobalt catalyst for C-N cross coupling reactions: synthesis of abemaciclib and fedratinib

Hajipour, Abdol R.,Khorsandi, Zahra,Sarfjoo, Mohamad Reza,Varma, Rajender S.

supporting information, p. 5222 - 5229 (2021/07/29)

Herein, the synthesis of a nano-catalytic system comprising magnetic nanoparticles as the core and edible natural ligands bearing functional groups as supports for cobalt species is described. Subsequent to its characterization, the efficiency of the catalyst was investigated for C-N cross-coupling reactions using assorted derivatives of amines and aryl halides. This novel and easily accessible Pd- and Cu-free catalyst exhibited good catalytic activity in these reactions using γ-valerolactone (GVL) at room temperature; good recyclability bodes well for the future application of this strategy. The introduced catalytic system is attractive in view of the excellent efficiency in an array of coupling reactions and its versatility is illustrated in the synthesis of abemaciclib and fedratinib, which are FDA-approved new and significant anti-cancer medicinal compounds that are prepared under green reaction conditions.

Intercalation of copper salt to montmorillonite K-10 and its application as a reusable catalyst for Chan–Lam cross-coupling reaction

Sarmah, Manashi,Dewan, Anindita,Boruah, Purna K.,Das, Manash R.,Bora, Utpal

, (2020/02/13)

A simple and efficient catalytic system has been developed by adsorption of copper salt in the interlayers of montmorillonite K-10. The catalytic system impressively exercises the green chemistry perspective leading to effortless recovery and recyclabilit

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