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1H-1,2,4-Triazole, 1-(4-methylphenyl)-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65814-58-6

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65814-58-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65814-58-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,1 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65814-58:
(7*6)+(6*5)+(5*8)+(4*1)+(3*4)+(2*5)+(1*8)=146
146 % 10 = 6
So 65814-58-6 is a valid CAS Registry Number.

65814-58-6SDS

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-(4-methylphenyl)-3-phenyl-1,2,4-triazole

1.2 Other means of identification

Product number -
Other names 3-Phenyl-1-(p-tolyl)-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:65814-58-6 SDS

65814-58-6Downstream Products

65814-58-6Relevant academic research and scientific papers

Metal-free Decarboxylative Annulation of 2-Aryl-2-isocyano-acetates with Aryldiazonium Salts: General Access to 1,3-Diaryl-1,2,4-triazoles

Tian, Yu-Ting,Zhang, Fa-Guang,Nie, Jing,Cheung, Chi Wai,Ma, Jun-An

, p. 227 - 233 (2021)

Isocyanoacetates are versatile substrates for the synthesis of heterocyclic compounds, but the concomitant decarboxylation remains rare. Herein we report a decarboxylative annulation reaction of 2-aryl-2-isocyanoacetates with aryldiazonium salts. This metal-free, base-promoted protocol allows for the access to a broad collection of 1,3-diaryl-1,2,4-triazoles, including chiral triazole-based binaphthalene ligands, drug mimics, and synthetic intermediates of druglike molecules. (Figure presented.).

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