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1-(1-(2-methylphenyl)cyclohexyl)piperidine is a complex organic compound with the molecular formula C18H27N. It features a piperidine ring, which is a six-membered nitrogen-containing ring, fused to a cyclohexane ring. One of the cyclohexane's phenyl groups is substituted with a methyl group at the 2nd position, and this phenyl group is connected to the piperidine ring. 1-(1-(2-methylphenyl)cyclohexyl)piperidine is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of certain drugs. It is also recognized for its psychoactive properties and has been studied for its effects on the central nervous system. Due to its complex structure and potential uses, 1-(1-(2-methylphenyl)cyclohexyl)piperidine is a subject of interest in chemical research and development.

2201-29-8

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2201-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2201-29-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2201-29:
(6*2)+(5*2)+(4*0)+(3*1)+(2*2)+(1*9)=38
38 % 10 = 8
So 2201-29-8 is a valid CAS Registry Number.

2201-29-8Downstream Products

2201-29-8Relevant academic research and scientific papers

Synthesis and preliminary biochemical evaluation of novel derivatives of PCP

Linders, Joannes T. M.,Furlano, David C.,Mattson, Mariena V.,Jacobson, Arthur E.,Rice, Kenner C.

scheme or table, p. 79 - 87 (2011/01/13)

(±)-Trans-Ph/Et and (±)-cis-Ph/Et 1-(2-ethyl-1- phenylcyclohexyl)piperidine were synthesized from 2-ethylcyclohexanone. In contrast to the corresponding trans-substituted 2-methyl compound which is 5x more potent than PCP, the trans-2-ethyl derivative has a 75x lower affinity for the PCP binding site. The cis-2-ethyl isomer is inactive like the cis-2-methyl derivative. (±)-1-(1-Phenylcyclohexyl)-2-methylpiperidine is almost as active as the parent PCP. Reduction of the aromatic ring or quaternization of the piperidine in PCP reduces the affinity for the PCP site.

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