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Diethyl quinoxaline-2,3-dicarboxylate is a chemical compound with the molecular formula C11H10N2O4. It is a white crystalline solid that is soluble in common organic solvents such as ethanol, acetone, and dichloromethane. diethyl quinoxaline-2,3-dicarboxylate is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is synthesized through the condensation of quinoxaline-2,3-dicarboxylic acid with ethanol in the presence of a catalyst. Diethyl quinoxaline-2,3-dicarboxylate is known for its stability and reactivity, making it a valuable building block in organic chemistry.

2379-59-1

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2379-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2379-59-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,7 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2379-59:
(6*2)+(5*3)+(4*7)+(3*9)+(2*5)+(1*9)=101
101 % 10 = 1
So 2379-59-1 is a valid CAS Registry Number.

2379-59-1Relevant academic research and scientific papers

PIDA/TBAB-Promoted Oxidative Geminal Dibromofunctionalization of Alkynes: Direct Synthesis of Geminal Diazides

Arepally, Sagar,Babu, Venkata Nagarjuna,Polu, Ashok,Sharada, Duddu S.

, p. 5700 - 5705 (2018)

PIDA/TBAB-promoted oxidative geminal diazidofunctionalization of alkynes has been described for the first time. The transformation demonstrates a mechanistically distinctive approach to access geminal diazides, in which TBAB plays a crucial role as brominating agent and for the in situ generation of tetrabutylammonium azide. Furthermore, we have demonstrated here the first cycloaminative strategy by tactically employing the two azides groups leading to quinoxalines and synthesis of bis-triazole derivatives via copper catalysis.

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