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1H-1,2,3-Triazole, 4-(4-ethylphenyl)- is an organic compound with the chemical formula C10H11N3. It is a derivative of 1,2,3-triazole, a five-membered heterocyclic ring containing three nitrogen atoms. The 4-(4-ethylphenyl)- group is attached to the triazole ring, which consists of a phenyl ring (a six-carbon aromatic ring) with an ethyl group (a two-carbon alkyl chain) attached to the para position (the fourth carbon). 1H-1,2,3-Triazole, 4-(4-ethylphenyl)- is known for its potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science, due to its unique chemical properties and reactivity. It can be synthesized through various methods, including the reaction of 4-ethylphenylhydrazine with nitrile and sodium azide. The compound is typically used as an intermediate in the synthesis of more complex molecules or as a building block in the development of new compounds with specific properties.

56527-22-1

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56527-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56527-22-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,2 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56527-22:
(7*5)+(6*6)+(5*5)+(4*2)+(3*7)+(2*2)+(1*2)=131
131 % 10 = 1
So 56527-22-1 is a valid CAS Registry Number.

56527-22-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-ethylphenyl)-2H-triazole

1.2 Other means of identification

Product number -
Other names 1,2,3-triazole analogue,11

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:56527-22-1 SDS

56527-22-1Downstream Products

56527-22-1Relevant academic research and scientific papers

Direct Synthesis of 4-Aryl-1,2,3-triazoles via I2-Promoted Cyclization under Metal- And Azide-Free Conditions

Geng, Xiao,Huang, Chun,Wang, Li-Sheng,Wu, An-Xin,Wu, Yan-Dong,Yu, Xiao-Xiao,Zhao, Peng,Zhou, You

, p. 13664 - 13672 (2021/10/01)

We herein report an iodine-mediated formal [2 + 2 + 1] cyclization of methyl ketones, p-toluenesulfonyl hydrazines, and 1-aminopyridinium iodide for preparation of 4-aryl-NH-1,2,3-triazoles under metal- and azide-free conditions. Notably, this is achieved

Cu-Catalyzed Site-Selective and Enantioselective Ring Opening of Cyclic Diaryliodoniums with 1,2,3-Triazoles

Chao, Zengyin,Ma, Mingming,Gu, Zhenhua

supporting information, p. 6441 - 6446 (2020/09/02)

A Cu-catalyzed enantioselective ring-opening/triazolylation reaction is reported. The reaction shows excellent chemoselectivity regarding the three different nitrogen atoms of 1,2,3-triazoles. The optically enriched axially chiral aryl iodides thus obtained were readily derivatized to different types of chiral phosphine ligands and their corresponding copper or palladium complexes.

Method of catalytically synthesizing 4-aryl-NH-1,2,3-triazole derivative under microwave radiation

-

Paragraph 0011; 0013, (2018/03/26)

The invention discloses a method of catalytically synthesizing 4-aryl-NH-1,2,3-triazole derivative under microwave radiation. The method includes the steps of: successively adding substituted 2-nitroolefin, sodium azide, TfOH, and pyridine into a reaction

Preparation of reusable Ag-decorated graphene oxide catalysts for decarboxylative cycloaddition

Kim, Ji Dang,Palani, Thiruvengadam,Kumar, Manian Rajesh,Lee, Sunwoo,Choi, Hyun Chul

, p. 20665 - 20670 (2013/02/22)

In this study, we demonstrated a noble Ag-decorated graphene oxide catalyst (GOSH-Ag) for use in the decarboxylative cycloaddition reaction. The catalyst was easily prepared by depositing Ag nanoparticles on thiolated graphene oxide (GOSH) surfaces. Trans

Compounds and methods

-

, (2008/06/13)

Compounds of this invention are non-peptide, reversible inhibitors of type 2 methionine aminopeptidase, useful in treating conditions mediated by angiogenesis, such as cancer, haemangioma, proliferative retinophathy, rheumatoid arthritis, atherosclerotic

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