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α-<3-<4-(1,2-benzisoxazol-3-yl)-1-piperazinyl>propyl>-4-fluorobenzenemethanol is a complex organic compound with a molecular formula of C22H24FN3O2. It is characterized by a benzisoxazole ring, a piperazine ring, and a fluorobenzene group, all connected through various carbon and nitrogen atoms. This chemical is known for its potential applications in the pharmaceutical industry, particularly as a precursor or intermediate in the synthesis of certain drugs. Its structure provides a unique set of properties that can be exploited for specific therapeutic effects. Due to its complexity, it is typically synthesized through multi-step organic reactions and requires careful handling and purification to ensure its purity and stability.

87757-02-6

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87757-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87757-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,5 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87757-02:
(7*8)+(6*7)+(5*7)+(4*5)+(3*7)+(2*0)+(1*2)=176
176 % 10 = 6
So 87757-02-6 is a valid CAS Registry Number.

87757-02-6Downstream Products

87757-02-6Relevant 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 (2007/10/02)

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.

Benzisothiazole and benzisoxazole piperazine derivatives

-

, (2008/06/13)

Disubstituted N,N-piperazinyl derivatives are disclosed wherein one substituent is benzisothiazol-3-yl or benzisoxazol-3-yl and the other is alkylene attached to heterocycles such as azaspiro[4.5]decanedione, dialkylglutarimide, thiazolidinedione and spirocyclopentylthiazolidinedione or butyrophenone-like groups. The compounds have psychotropic properties and 8-[4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl]-8-azaspior[4.5]decane-7,9-dione is a typical embodiment having selective antipsychotic activity.

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