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1-m-Trifluormethylphenylcyclohexanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60652-07-5

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60652-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60652-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,5 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60652-07:
(7*6)+(6*0)+(5*6)+(4*5)+(3*2)+(2*0)+(1*7)=105
105 % 10 = 5
So 60652-07-5 is a valid CAS Registry Number.

60652-07-5Relevant academic research and scientific papers

BACE-2 INHIBITORY COMPOUNDS AND RELATED METHODS OF USE

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Paragraph 0200; 0201, (2017/05/02)

Provided herein are novel compounds of Formulae I-III, and methods of using the same to selectively inhibit BACE2.

Synthesis and Anticonvulsant Activity of 1-Phenylcyclohexylamine Analogues

Thurkauf, Andrew,Costa, Brian de,Yamaguchi, Shun-ichi,Mattson, Mariena V.,Jacobson, Arthur E.,et al.

, p. 1452 - 1458 (2007/10/02)

Thirty-eight analogues of 1-phenylcyclohexylamine (PCA), a phencyclidine (PCP) derivative, were examined for their activities in the mouse maximal electroshock (MES) seizure test and in a motor-toxicity assay.In addition, we determined the binding affinities of the compounds for PCP acceptor sites in rat brain membranes labeled with -1-piperidine.Many of the analogues were protective against MES seizures (ED50s of 4-41 mg/kg, ip) and all of these compounds caused motor toxicity.The potencies in the motor toxicity and MES seizure tests showed a moderate correlation with the affinities for PCP sites.Several analogues exhibited a greater separation of potencies in the motor toxicity and MES seizure tests than did the parent compound PCA.These were obtained by (i) 3-methylation of the cyclohexyl ring trans to the phenyl ring, (ii) methoxylation at the ortho position on the phenyl ring, and (iii) contraction of the cyclohexane ring to form the corresponding cyclopentane.

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