36938-76-8 Usage
Uses
Used in Pharmaceutical Synthesis:
4-(4-CHLOROBENZYL)PIPERIDINE is used as a key component in the synthesis of various pharmaceuticals and drug intermediates, leveraging its unique chemical structure to contribute to the development of new medications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 4-(4-CHLOROBENZYL)PIPERIDINE is utilized as a building block for the creation of new psychoactive substances, indicating its role in advancing the understanding and treatment of various psychological conditions.
Used in Antipsychotic Drug Development:
4-(4-CHLOROBENZYL)PIPERIDINE is employed as a precursor in the development of antipsychotic drugs, where its structure may contribute to the modulation of neurotransmitter activity and the treatment of psychotic disorders.
Used in Central Nervous System Agents:
Depending on its modification, 4-(4-CHLOROBENZYL)PIPERIDINE has potential applications as a central nervous system stimulant or depressant, highlighting its versatility in pharmacological research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 36938-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,3 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36938-76:
(7*3)+(6*6)+(5*9)+(4*3)+(3*8)+(2*7)+(1*6)=158
158 % 10 = 8
So 36938-76-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H16ClN/c13-12-3-1-10(2-4-12)9-11-5-7-14-8-6-11/h1-4,11,14H,5-9H2
36938-76-8Relevant academic research and scientific papers
The synthesis of substituted bipiperidine amide compounds as CCR3 antagonists
Ting, Pauline C.,Lee, Joe F.,Wu, Jie,Umland, Shelby P.,Aslanian, Robert,Cao, Jianhua,Dong, Youhao,Garlisi, Charles G.,Gilbert, Eric J.,Huang, Ying,Jakway, James,Kelly, Joseph,Liu, Zhidan,McCombie, Stuart,Shah, Himanshu,Tian, Fang,Wan, Yuntao,Shih, Neng-Yang
, p. 1375 - 1378 (2007/10/03)
Bipiperidine amide 1 has been identified as a CC chemokine receptor 3 (CCR3) antagonist. Optimization of its structure-activity relationship has resulted in the identification of cis (R,R)-4-[(3,4-dichlorophenyl)methyl]-3- hydroxymethyl-1′(6-quinolinylcar
