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Piperidine, 1-acetyl-4-(2,4-dichlorobenzoyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84162-85-6

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84162-85-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84162-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,1,6 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84162-85:
(7*8)+(6*4)+(5*1)+(4*6)+(3*2)+(2*8)+(1*5)=136
136 % 10 = 6
So 84162-85-6 is a valid CAS Registry Number.

84162-85-6Relevant academic research and scientific papers

DUAL MODULATORS OF 5HT2A AND D3 RECEPTORS

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Page/Page column 41, (2009/02/11)

The present invention relates to compounds of the formula (I) wherein R1, R2, X and n are as defined in the specification as dual modulators of the serotonin 5-HT2a and dopamine D3 receptors, their manufacture,

Benzoyl-piperidine derivatives as dual modulators of the 5-HT2A and D3 receptors

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Page/Page column 53, (2010/11/28)

The present invention relates to compounds of the general formula as dual modulators of the 5-HT2a and D3 receptors useful against CNS disorders, wherein A, R1, R2, n, p, q and r are as defined in the specificat

Synthesis and Neuroleptic Activity of 3-(1-Substituted-4-piperidinyl)-1,2-benzisoxazoles

Strupczewski, Joseph T.,Allen, Richard C.,Gardner, Beth Ann,Schmid, Blaine L.,Stache, Ulrich,et al.

, p. 761 - 769 (2007/10/02)

The synthesis of a series of 3-(1-substituted-4-piperidinyl)-1,2-benzisoxazoles is described.The neuroleptic activity of the series was evaluated by utilizing the climbing mice assay and inhibition of spiroperidol binding.Structure-activity relationships were studied by variation of the substituent on the benzisoxazole ring with concomitant variation of four different 1-piperidinyl substituents.Maximum neuroleptic activity was realized when there was a 6-fluoro substituent on the benzisoxazole ring.The 1-piperidinyl substituent appeared less significant, although in most cases, the (1,3-dihydro-2-oxo-2H-benzimidazol-1-yl)propyl group imparted maximum potency.The most potent compound in both assays was 6-fluoro-3--4-piperidinyl>-1,2-benzisoxazole (11b).

3-(4-Piperidyl)-1,2-benzisoxales

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, (2008/06/13)

Novel 3-(4-piperidyl)-1,2-benzisoxazoles, intermediates and processes for the preparation thereof, and methods for alleviating pain utilizing compounds or compositions thereof are disclosed.

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