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1-Benzyl-4-(naphthalen-2-yl)piperazine is a synthetic organic compound with the molecular formula C21H21N3. It is a derivative of piperazine, a heterocyclic amine, and features a benzyl group attached to the 1-position and a naphthalen-2-yl group at the 4-position. 1-benzyl-4-(naphthalen-2-yl)piperazine is known for its potential psychoactive effects and has been studied for its interactions with the serotonin system in the brain. Due to its complex structure and pharmacological properties, it is primarily of interest in scientific research and not approved for medical use. It is important to note that the compound is not intended for human consumption and its distribution and possession may be subject to legal restrictions depending on the jurisdiction.

1620-35-5

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1620-35-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1620-35-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1620-35:
(6*1)+(5*6)+(4*2)+(3*0)+(2*3)+(1*5)=55
55 % 10 = 5
So 1620-35-5 is a valid CAS Registry Number.

1620-35-5Downstream Products

1620-35-5Relevant academic research and scientific papers

Synthesis of N-alkyl-N′-aryl or Alkenylpiperazines: A Copper-Catalyzed C–N Cross-Coupling in the Presence of Aryl and Alkenyl Triflates and DABCO

Ghazanfarpour-Darjani, Majid,Barat-Seftejani, Forugh,Khalaj, Mehdi,Mousavi-Safavi, Seyed Mahmoud

, (2017)

Unsymmetrical piperazines are key constituents of many pharmaceuticals. Given that the selective introduction of an aryl and alkyl motif onto the piperazine is not always straightforward, direct arylation and alkenylation of 1,4-diaza-bicyclo[2.2.2]octane would obviate the inefficiencies associated with the preparation of these target molecules. We have utilized alkyl halides, aryl or alkenyl triflates, and 1,4-diaza-bicyclo[2.2.2]octane for the synthesis of N-alkyl-N′-aryl or alkenylpiperazines. The optimum conditions are developed using CuCl, t-BuOLi in NMP. Alkenyl triflates requires N,N′-dimethylethylenediamine and higher temperature to afford the desired cross-coupled product. Substrates bearing electron-deficient and electron-rich groups were successfully coupled under the optimum reaction conditions.

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