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6,7-dichloro-3-(4-chloro-phenyl)-1H-quinoxalin-2-one is a complex organic compound with the molecular formula C14H7Cl3N2O. It is a derivative of quinoxaline, a fused bicyclic aromatic heterocyclic compound consisting of a benzene ring fused to a diazine ring. The compound features two chlorine atoms at the 6 and 7 positions, a 4-chlorophenyl group attached at the 3 position, and a carbonyl group at the 2 position. This chemical is known for its potential applications in pharmaceuticals and materials science, particularly in the development of new drugs and as a building block for more complex molecules. Due to its halogenated nature, it may also be of interest in the synthesis of other organic compounds.

4017-10-1

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4017-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4017-10-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,1 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4017-10:
(6*4)+(5*0)+(4*1)+(3*7)+(2*1)+(1*0)=51
51 % 10 = 1
So 4017-10-1 is a valid CAS Registry Number.

4017-10-1Downstream Products

4017-10-1Relevant academic research and scientific papers

Asymmetric organocatalytic tandem cyclization/transfer hydrogenation: A synthetic strategy for enantioenriched nitrogen heterocycles

Shi, Feng,Tan, Wei,Zhang, Hong-Hao,Li, Mei,Ye, Qin,Ma, Guan-Hua,Tu, Shu-Jiang,Li, Guigen

, p. 3715 - 3726 (2013)

An asymmetric organocatalytic tandem reaction comprising cyclization/transfer hydrogenation has been established in a compatible and synergistic way, leading to the step-economical synthesis of enantioenriched tetrahydroquinoxalines and dihydroquinoxalinones from readily accessible materials in excellent enantioselectivity of up to >99% ee. This protocol of a one-operation tandem reaction combines the merits of both tandem reactions and asymmetric organocatalysis, providing an efficient strategy for concisely and enantioselectively synthesizing nitrogen heterocycles with biological relevance. Copyright

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