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1,4-di-naphthalen-1-yl-piperazine is a complex organic compound with the molecular formula C24H18N2. It is characterized by two naphthalene rings attached to the 1,4-positions of a piperazine molecule, which is a heterocyclic amine containing two nitrogen atoms in a six-membered ring. 1,4-di-naphthalen-1-yl-piperazine is known for its potential applications in the synthesis of pharmaceuticals and as a building block in the creation of more complex organic molecules. Due to its specific structure, it may exhibit unique chemical properties and reactivity, making it a subject of interest in organic chemistry research.

3367-55-3

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3367-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3367-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3367-55:
(6*3)+(5*3)+(4*6)+(3*7)+(2*5)+(1*5)=93
93 % 10 = 3
So 3367-55-3 is a valid CAS Registry Number.

3367-55-3Downstream Products

3367-55-3Relevant academic research and scientific papers

Synthesis of N-arylpiperazines from aryl halides and piperazine under a palladium tri-tert-butylphosphine catalyst

Nishiyama, Masakazu,Yamamoto, Toshihide,Koie, Yasuyuki

, p. 617 - 620 (1998)

A Pd/P(t-Bu), catalyst system has revealed very high activity and selectivity for the amination of N-(hetero)aryl halides with unprotected piperazine. A wide variety of N-(hetero)arylpiperazines could be prepared using this catalyst. Turnover numbers up to 6400mol/mol have been obtained.

Nickel-catalysed selective N-arylation or N,N′-diarylation of secondary diamines

Brenner, Eric,Schneider, Rapha?l,Fort, Yves

, p. 6913 - 6924 (2007/10/03)

The selective synthesis of N-aryl or N,N′-diaryl piperazines and trimethylene(bis)piperidines from the corresponding diamines and aryl chlorides using a catalyst combination of Ni(0) associated to 2,2′-bipyridine is described. The Ni/2,2′-bipyridine catalyst is also effective for the sequential arylation of piperazine. The preparation of novel and unsymmetrical 1,4-diaryl piperazines is reported.

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