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Quinoxaline, 2,3-diethyl- is a heterocyclic organic compound with the chemical formula C9H10N2. It is a derivative of quinoxaline, which is a fused bicyclic ring system consisting of a benzene ring and a pyrazine ring. The 2,3-diethyl substitution refers to the presence of two ethyl groups attached to the second and third carbon atoms of the quinoxaline core. Quinoxaline, 2,3-diethyl- is known for its potential applications in pharmaceuticals and agrochemicals, as well as its use as a building block in the synthesis of various heterocyclic compounds. It is typically synthesized through various methods, including condensation reactions, and is characterized by its unique chemical properties and reactivity.

3508-83-6

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3508-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3508-83-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,0 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3508-83:
(6*3)+(5*5)+(4*0)+(3*8)+(2*8)+(1*3)=86
86 % 10 = 6
So 3508-83-6 is a valid CAS Registry Number.

3508-83-6Downstream Products

3508-83-6Relevant academic research and scientific papers

CaO-catalyzed aerobic oxidation of α-hydroxy ketones: Application to one-pot synthesis of quinoxaline derivatives

Hara, Takayoshi,Takami, Yukihiro,Ichikuni, Nobuyuki,Shimazu, Shogo

experimental part, p. 488 - 490 (2012/08/07)

The aerobic oxidation of α-hydroxy ketones into α-diketones catalyzed by CaO is compared with the same reaction catalyzed by other metal oxides. The catalytic activities of the various metal oxides were proportional to their surface basicities. The direct conversion of α-hydroxy ketones into quinoxalines via CaO-catalyzed aerobic oxidation followed by in situ reaction with 1,2-diaminoaromatics is also achieved. Various types of quinoxalines were synthesized in the presence of the CaO catalyst and molecular oxygen. It was also found that the CaO catalyst was reusable without any loss of its catalytic activity.

The synthesis of quinoxalines by condensation reaction of acyleins with o-phenylenediamine without solvent under microwave irradiation

Juncai, Feng,Yang, Liu,Qinghua, Meng,Bin, Liu

, p. 193 - 196 (2007/10/03)

A convenient synthetic method for 2,3-disubstituted quinoxalines is described. Heating the aryl or alkyl acyloins and o-phenylenediamine in a microwave oven for 3-6 minutes affords 2,3-disubstituted quinoxalines in 20-94% yields.

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