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4073-72-7

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4073-72-7 Usage

General Description

3,4,5-Triphenyl-1,2,4-triazole is a chemical compound with the molecular formula C18H13N3. It is a white solid at room temperature and is used as a building block in the synthesis of various organic compounds. 3,4,5-TRIPHENYL-1,2,4-TRIAZOLE is commonly used in research and development processes, as well as in the production of pharmaceuticals, dyes, and other industrial chemicals. It has the potential for various applications in the fields of materials science, chemical engineering, and medicinal chemistry due to its unique chemical properties and versatile reactivity. Additionally, studies have shown that 3,4,5-Triphenyl-1,2,4-triazole exhibits significant biological activities, making it a potential candidate for drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 4073-72-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4073-72:
(6*4)+(5*0)+(4*7)+(3*3)+(2*7)+(1*2)=77
77 % 10 = 7
So 4073-72-7 is a valid CAS Registry Number.

4073-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,5-TRIPHENYL-1,2,4-TRIAZOLE

1.2 Other means of identification

Product number -
Other names 3,4,5-Triphenyl-4H-1,2,4-triazol

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:4073-72-7 SDS

4073-72-7Relevant articles and documents

Cationic Iridium Complexes with 3,4,5-Triphenyl-4 H-1,2,4-Triazole Type Cyclometalating Ligands: Synthesis, Characterizations, and Their Use in Light-Emitting Electrochemical Cells

Bai, Rubing,Chen, Mengzhen,He, Lei,Meng, Xianwen

, (2020/08/05)

Cationic iridium complexes that show blue-shifted emission and high phosphorescent efficiency have been pursued for their optoelectronic applications. Five cationic iridium complexes with 3,4,5-triphenyl-4H-1,2,4-triazole (tPhTAZ) type cyclometalating ligands (C^N) and 2,2′-bipyridine or 2-(pyridin-2-yl)-1H-benzo[d]imidazole type ancillary ligands (N^N) have been designed and synthesized. Their structures have been confirmed by X-ray crystallography, and their photophysical and electrochemical properties have been comprehensively characterized. In solution and thin films, the complexes afford efficient yellow to blue-green emission. The highest occupied molecular orbitals (HOMOs) of these complexes are delocalized over the C^N ligand and the iridium ion, and compared with the conventional 2-phenylpyridine (Hppy) ligand, the tPhTAZ ligand largely shifts the emission of the complex toward blue by over 40 nm through stabilizing the HOMO. Moreover, the peripheral phenyl rings in tPhTAZ provide steric hindrance to the complexes, which suppresses phosphorescence concentration-quenching of the complexes, leading to high luminescent efficiencies in neat films. Theoretical calculations have shown that the emission of the complexes originates from either the charge-transfer state (Ir/C^N → N^N) or the C^N/N^N-centered 3π-π? state, depending on the local surrounding of the complex. The complexes exhibit good electrochemical stability with reversible oxidation and reduction processes in solution. Solid-state light emitting electrochemical cells (LECs) using the complexes afford yellow to blue-green emission, with peak current efficiencies of up to 34.7 cd A-1 and maximum brightness of up to 256 cd m-2 at 3.0 V, which are among the highest for LECs based on cationic iridium complexes reported so far, indicating the great potential for the use of tPhTAZ-type C^N ligands in construction of cationic iridium complexes for LEC applications.

A simple and efficient synthesis of 3,4,5-trisubstituted/N-fused 1,2,4-triazoles via ceric ammonium nitrate catalyzed oxidative cyclization of amidrazones with aldehydes using polyethylene glycol as a recyclable reaction medium

Nakka, Mangarao,Tadikonda, Ramu,Rayavarapu, Srinuvasarao,Sarakula, Prasanthi,Vidavalur, Siddaiah

, p. 517 - 525 (2015/02/19)

An environmentally benign protocol is described for the synthesis of 3,4,5-trisubstituted 1,2,4-triazoles and N-fused 1,2,4-triazoles via ceric ammonium nitrate catalyzed oxidative cyclization of amidrazones and aldehydes using polyethylene glycol as recyclable reaction medium. This protocol is effective toward various substrates having different functionalities. The easy recyclability of the reaction medium makes the process economic and potentially viable for commercial applications.

Br?nsted acid-catalyzed simple and efficient synthesis of 1,2,4-triazoles and 1,2,4-oxadiazoles using 2,2,2-trichloroethyl imidates in PEG

Mangarao, Nakka,Mahaboob Basha, Gajula,Ramu, Tadikonda,Srinuvasarao, Rayavarapu,Prasanthi, Sarakula,Siddaiah, Vidavalur

supporting information, p. 177 - 179 (2014/01/06)

A facile and highly efficient synthesis of 3,4,5-trisubstituted 1,2,4-triazoles and 3,5-disubstituted 1,2,4-oxadiazoles from 2,2,2-trichloroethyl imidates using PEG as a solvent and employing PTSA as the catalyst under mild conditions is described.

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