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2-phenyl-1-(2-phenylpyrrolidin-1-yl)ethan-1-one is a complex organic compound with the molecular formula C20H21NO. It features a phenyl group (C6H5) attached to the 2-position of an ethanone (acetophenone) backbone, which is further substituted at the 1-position with a pyrrolidinyl group. The pyrrolidinyl group itself has a phenyl group attached to its 2-position, creating a unique structure with two phenyl rings and a five-membered nitrogen-containing ring. 2-phenyl-1-(2-phenylpyrrolidin-1-yl)ethan-1-one is of interest in the field of organic chemistry, potentially for its pharmaceutical or chemical properties, although specific applications or uses are not detailed in this summary.

1032-33-3

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1032-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1032-33-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,3 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1032-33:
(6*1)+(5*0)+(4*3)+(3*2)+(2*3)+(1*3)=33
33 % 10 = 3
So 1032-33-3 is a valid CAS Registry Number.

1032-33-3Relevant academic research and scientific papers

Benzaldehyde- And Nickel-Catalyzed Photoredox C(sp3)-H Alkylation/Arylation with Amides and Thioethers

Si, Xiaojia,Zhang, Lumin,Hashmi, A. Stephen K.

, p. 6329 - 6332 (2019)

Herein a synergistic combination of a nickel catalyst and benzaldehyde for the utilization of amides and thioethers in C(sp3)-H alkylation and arylation reactions employing simple aryl or alkyl halides is reported. This method provides a simple and cheap strategy for the direct functionalization of amides and thioethers. Readily available starting materials, mild reaction conditions, a good functional-group tolerance, and a broad substrate scope make this methodology attractive and practical for pharmaceutical and synthetic chemistry.

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