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4-(4-phenylpiperazin-1-yl)butanenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25220-31-9

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25220-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25220-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,2 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25220-31:
(7*2)+(6*5)+(5*2)+(4*2)+(3*0)+(2*3)+(1*1)=69
69 % 10 = 9
So 25220-31-9 is a valid CAS Registry Number.

25220-31-9Relevant academic research and scientific papers

Synthesis and pharmacological evaluation of [(4-Arylpiperazin-1-yl)-alkyl]- carbamic acid ethyl ester derivatives as potential anxiolytic agents

Khatri, Manisha,Rai, Santosh K.,Ranbhor, Ranjit,Kishore, Krishna,Tiwari, Manisha

experimental part, p. 1143 - 1152 (2012/11/07)

On the basis of our earlier studies, a series of N-{4-[4-(aryl) piperazin-1-yl]-phenyl}-amine derivatives containing terminal carbamoyl fragment with alkyl spacer of different lengths (15-20) were synthesized as ligands, for 5-hydroxytryptamine-1A (5-HT1A

Further structure-activity relationships study of hybrid 7-{[2-(4-phenylpiperazin-1-yl)ethyl]propylamino}-5,6,7,8-tetrahydronaphthalen-2- ol analogues: identification of a high-affinity D3-preferring agonist with potent in vivo activity with long duration

Biswas, Swati,Zhang, Suhong,Fernandez, Fernando,Ghosh, Balaram,Zhen, Juan,Kuzhikandathil, Eldo,Reith, Maarten E. A.,Dutta, Aloke K.

, p. 101 - 117 (2008/09/20)

This paper describes an extended structure-activity relationships study of aminotetralin-piperazine-based hybrid molecules developed earlier for dopamine D2/D3 receptors. Various analogues as positional isomers have been developed where location of the ph

Synthesis of arylpiperazines with a terminal naphthothiazole group and their evaluation on 5-HT, DA and α receptors

Perrone,Berardi,Colabufo,Tortorella,Fornaretto,Caccia,McArthur

, p. 739 - 746 (2007/10/03)

The synthesis, affinities for 5-HT(1A), 5-HT2, D1, D2, α1 and α2 receptors and structure-activity relationships are described for a series of arylpiperazines substituted on the N-4 atom with an ω-(2-n

Anthelmintic 1-(substituted phenyl)-3-alkanimidoyl ureas

-

, (2008/06/13)

The compounds of this invention are novel imidoylureas having anthelmintic activity and imidoylthioureas having antifertility activity. They are prepared by the reaction of appropriate amidines with appropriate isocyanates or isothiocyanates.

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