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3-Ethyl-6-methyl[1,2,4]triazolo[4,3-a]pyridine is a heterocyclic compound characterized by a triazole ring fused to a pyridine ring. The structure features an ethyl group at the 3-position and a methyl group at the 6-position, which are both substituents on the pyridine ring. 3-ethyl-6-methyl[1,2,4]triazolo[4,3-a]pyridine is of interest in organic chemistry and may have potential applications in the development of pharmaceuticals or agrochemicals due to its unique structure and the ability to form various derivatives. The specific properties, reactivity, and applications of 3-ethyl-6-methyl[1,2,4]triazolo[4,3-a]pyridine would depend on its chemical environment and the context in which it is used.

4919-19-1

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4919-19-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4919-19-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,1 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4919-19:
(6*4)+(5*9)+(4*1)+(3*9)+(2*1)+(1*9)=111
111 % 10 = 1
So 4919-19-1 is a valid CAS Registry Number.

4919-19-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-CRESOTIC ACID,3-ETHYL

1.2 Other means of identification

Product number -
Other names 3-Ethyl-2,6-cresotic acid

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:4919-19-1 SDS

4919-19-1Downstream Products

4919-19-1Relevant academic research and scientific papers

I2-TBHP-catalyzed one-pot highly efficient synthesis of 4,3-fused 1,2,4-triazoles from: N -tosylhydrazones and aromatic N-heterocycles via intermolecular formal 1,3-dipolar cycloaddition

Inturi, Surendra Babu,Kalita, Biswajit,Ahamed, A. Jafar

supporting information, p. 11061 - 11064 (2016/12/07)

I2-TBHP-catalyzed azomethine imine generation and subsequent regioselective 1,3-dipolar cycloaddition (DC) with aromatic N-heterocycles was developed to afford various 4,3-fused 1,2,4-triazoles in excellent yields. The method is operationally simple and highly efficient with broad functional group tolerance.

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