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Pyridine, 2-(5-methyl-3-phenyl-1H-1,2,4-triazol-1-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88974-93-0

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88974-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88974-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,7 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88974-93:
(7*8)+(6*8)+(5*9)+(4*7)+(3*4)+(2*9)+(1*3)=210
210 % 10 = 0
So 88974-93-0 is a valid CAS Registry Number.

88974-93-0SDS

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-(5-methyl-3-phenyl-1,2,4-triazol-1-yl)pyridine

1.2 Other means of identification

Product number -
Other names 1-(2-pyridyl)-3-phenyl-5-methyl-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:88974-93-0 SDS

88974-93-0Downstream Products

88974-93-0Relevant academic research and scientific papers

Electrochemical Synthesis of Heterocyclic Compounds. XV. Anodic Synthesis of s-Triazolopyridine Derivatives

Crljenak, Senka,Tabakovic, Ibro,Jeremic, Dragoslav,Gaon, Igor

, p. 527 - 536 (2007/10/02)

Anodic oxidation of several heterocyclic hydrazones (1a - 9a) prepared from 2-hydrazinopyridine of 2-hydrazino-4-nitropyridine and the corresponding aromatic aldehyde was performed in a CH3CN-Et4NClO4 solution with the addition of 60percent HClO4 on a platinum electrode, using controlled potentials.As a result of two-electron oxidative cyclizations, several s-triazolopyridine derivatives (1b - 9b) were prepared in yields ranging from 55 to 92percent.A mechanism rationalizing the formation of the 3-phenyl-s-triazolopyridine, 1b, has been studied by LSV, CPSV, RDE, coulometry and preparative scale electrolysis.

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