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3-methyl-4-phenyl-pyrrole-2,5-dione is a chemical compound with the molecular formula C12H9NO2. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with two carbon atoms and two nitrogen atoms. In this specific compound, a methyl group (-CH3) is attached to the third carbon atom, and a phenyl group (C6H5) is connected to the fourth carbon atom. The 2,5-dione part of the name indicates the presence of two carbonyl groups (C=O) at the second and fifth positions of the pyrrole ring. 3-methyl-4-phenyl-pyrrole-2,5-dione is known for its potential applications in the synthesis of various pharmaceuticals and organic compounds, as well as its role as an intermediate in chemical reactions.

5109-46-6

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5109-46-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5109-46-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,0 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5109-46:
(6*5)+(5*1)+(4*0)+(3*9)+(2*4)+(1*6)=76
76 % 10 = 6
So 5109-46-6 is a valid CAS Registry Number.

5109-46-6Downstream Products

5109-46-6Relevant academic research and scientific papers

Pd-Catalyzed α-Selective C-H Functionalization of Olefins: En Route to 4-Imino-β-Lactams

Kong, Wei-Jun,Liu, Yue-Jin,Xu, Hui,Chen, Yan-Qiao,Dai, Hui-Xiong,Yu, Jin-Quan

, p. 2146 - 2149 (2016/03/05)

Pd-catalyzed α-olefinic C-H activation of simple α,β-unsaturated olefins has been developed. 4-imino-β-lactam derivatives were readily synthesized via activation of α-olefinic C-H bonds with excellent cis stereoselectivity. A wide range of heterocycles at the β-position are compatible with this reaction. The product of 4-imino-β-lactam derivatives can be readily converted to 2-aminoquinoline which exists extensively in pharmaceutical drugs and natural products.

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