60814-29-1 Usage
Description
2,6-dimethylquinoxaline is a heterocyclic aromatic compound characterized by a quinoxaline core structure with two methyl groups at the 2nd and 6th positions. It has the molecular formula C10H10N2 and is known for its versatile physicochemical properties, including its potential as a ligand in coordination chemistry and its biological activities. 2,6-dimethylquinoxaline is also found in certain natural products and has been studied for its applications in materials science and catalysis.
Uses
Used in Pharmaceutical and Agrochemical Industries:
2,6-dimethylquinoxaline is utilized as a building block in the synthesis of various organic compounds, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure and properties contribute to the creation of novel and effective molecules for these industries.
Used in Coordination Chemistry:
As a ligand, 2,6-dimethylquinoxaline is employed in coordination chemistry to form complexes with metal ions. This application allows for the exploration of its properties and potential uses in various chemical and catalytic processes.
Used in Materials Science:
2,6-dimethylquinoxaline has been studied for its potential applications in materials science, where its unique properties can be harnessed to develop new materials with specific characteristics for various uses.
Used in Catalysis:
2,6-dimethylquinoxaline has also been identified for its potential applications in catalysis, where it can act as a catalyst or a catalyst support, facilitating chemical reactions and improving their efficiency.
Check Digit Verification of cas no
The CAS Registry Mumber 60814-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,1 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60814-29:
(7*6)+(6*0)+(5*8)+(4*1)+(3*4)+(2*2)+(1*9)=111
111 % 10 = 1
So 60814-29-1 is a valid CAS Registry Number.
60814-29-1Relevant articles and documents
The Thermolysis of Polyazapentadienes. Part 3. Cyclisation of C-Methyl-1,2,5-triazapentadienes and Related Compounds: The Role of an Intermediate Spirodienyl Radical
McNab, Hamish
, p. 371 - 376 (2007/10/02)
A series of C-methyl-1,2,5-triazapentadienes and 2,5-diaza-1-oxapentadienes are prepared from pyruvaldehyde phenylhydrazones and oxime anils respectively.The 4-methyl derivatives show E/Z isomerism about the 4,5-double bond.Pyrolysis of the 5-phenyl derivatives (1), (3), (5), (7), and (10) causes cyclisation to 2-methylquinoxaline, though 2-phenyliminopropanonitrile is obtained from the oxime ester (9).Pyrolysis of the 5-p-tolyl derivatives (2), (4), (6), (8), and (11) qives mixtures of 2,6- and 2,7-dimethylquinoxaline.There are formed predominantly by the rearrangement reaction which involves the spirodienyl radical (19), but also by direct cyclisation of the iminyl radicals (17) and (18).
