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2-phenyl-3-(pyrrolidin-1-yl)-1H-inden-1-one is a complex organic compound with the molecular formula C20H19NO. It is a derivative of inden-1-one, featuring a phenyl group at the 2-position and a pyrrolidin-1-yl group at the 3-position. 2-phenyl-3-(pyrrolidin-1-yl)-1H-inden-1-one is characterized by its unique structure, which includes a fused ring system with a carbonyl group at the 1-position. It is a white to off-white crystalline solid and is typically synthesized through various chemical reactions involving indenones and amines. Due to its specific structure, it may have potential applications in the field of pharmaceuticals or as a building block for more complex organic molecules. However, its exact uses and properties would depend on further research and characterization.

1953-63-5

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1953-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1953-63-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,5 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1953-63:
(6*1)+(5*9)+(4*5)+(3*3)+(2*6)+(1*3)=95
95 % 10 = 5
So 1953-63-5 is a valid CAS Registry Number.

1953-63-5Downstream Products

1953-63-5Relevant academic research and scientific papers

Cs2CO3 Catalyzed Intramolecular Aminocarbonylation of Alkynes: Synthesis of 3-Amino-1H-inden-1-ones from N-tert-Butyl-2-(1-alkynyl)benzaldimines

Guo, Zhen,Liu, Tao,Liang, Xiujuan,Wu, Yuting,Yao, Tuanli

, p. 1053 - 1057 (2020)

Synthesis of a wide variety of 3-amino-1H-inden-1-ones from N-tert-butyl-2-(1-alkynyl)benzaldimines via intramolecular aminocarbonylation of alkynes using Cs2CO3 as catalyst and air as oxidant has been developed. This highly atom-efficient, transition-metal-free reaction proceeds under thermal conditions. We propose that the reaction proceeds through an unprecedented 5-exo-dig cyclization of N-tert-butyl-2-(1-alkynyl)benzaldimines and thermal rearrangement of 3-methylene-2λ2-isoindolin-1-ols. (Figure presented.).

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