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α-<3-<4-(1,2-benzisothiazol-3-yl)-1-piperazinyl>propyl>-4-fluorobenzenemethanol is a complex organic compound with a molecular formula of C22H24FN3OS2. It is characterized by a benzisothiazol-3-yl group attached to a piperazinyl moiety, which is further connected to a propyl chain and a 4-fluorobenzenemethanol group. This chemical structure suggests potential applications in pharmaceuticals or as a chemical intermediate due to its unique arrangement of functional groups. The compound's properties, such as solubility and reactivity, would be influenced by the presence of the fluorine atom, the benzisothiazole ring, and the piperazine group, making it a compound of interest for further study in chemical research and development.

87692-10-2

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87692-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87692-10-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,9 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87692-10:
(7*8)+(6*7)+(5*6)+(4*9)+(3*2)+(2*1)+(1*0)=172
172 % 10 = 2
So 87692-10-2 is a valid CAS Registry Number.

87692-10-2Downstream Products

87692-10-2Relevant academic research and scientific papers

Synthesis and Biological Evaluation of 1-(1,2-Benzisothiazol-3-yl)- and (1,2-Benzisoxazol-3-yl)piperazine Derivatives as Potential Antipsychotic Agents

Yevich, Joseph P.,New, James S.,Smith, David W.,Lobeck, Walter G.,Catt, John D.,et al.

, p. 359 - 369 (1986)

Members of the series of title compounds were tested for potential antipsychotic activity in relevant receptor binding assays and behavioral screens.Structure-activity relationships within the series are discussed.Compound 24 (BMY 13859-1), a (1,2-benzisothiazol-3-yl)piperazine derivative, was selected for further study because of its potent and selective profile in primary CNS tests.It was active in the Sidman avoidance paradigm and blocked amphetamine-induced stereotyped behavior in dogs for up to 7 h.The compound's lack of typical neuroleptic-like effects in therat catalepsy test and its failure to produce dopamine receptor supersensitivity following chronic administration indicate that it should not cause the movement disorders commonly associated with antipsychotic therapy.Although 24 has potent affinity for dopaminergic binding sites, its even greater affinity for serotonin receptors suggests that a serotonergic component may be relevant to its atypical profile.Compound 24 is currently undergoing clinical evaluation in schizophrenic patients.

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