80843-96-5 Usage
Uses
Used in Pharmaceutical Industry:
MK-7264 is used as a potential treatment for insomnia and other sleep-related conditions due to its selective antagonistic action on the orexin-2 receptor. By inhibiting the activity of this receptor, it is believed to promote sleep and relaxation, making it a promising candidate for the development of new therapies to address sleep disorders.
Used in Clinical Research:
MK-7264 is currently being investigated in clinical trials to assess its safety, efficacy, and potential as a treatment for insomnia and other sleep-related conditions. The results of these trials will provide valuable information on the compound's therapeutic potential and may lead to the development of new medications for sleep disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 80843-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,4 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 80843-96:
(7*8)+(6*0)+(5*8)+(4*4)+(3*3)+(2*9)+(1*6)=145
145 % 10 = 5
So 80843-96-5 is a valid CAS Registry Number.
InChI:InChI=1/C25H28O3/c1-19-8-10-21(11-9-19)25(2,3)18-27-17-20-6-5-7-24(16-20)28-23-14-12-22(26-4)13-15-23/h5-16H,17-18H2,1-4H3
80843-96-5Relevant academic research and scientific papers
2-Arylpropyl ether or thioether derivatives and insecticidal and acaricidal agents containing said derivatives
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, (2008/06/13)
The present invention relates to 2-arylpropyl ether or thioether derivatives represented by the following general formula [I]: STR1 wherein Ar stands for an aryl group, R stands for a methyl or ethyl group, Y stands for an oxygen or sulfur atom, and B stands for a group represented by the following formula [II]: STR2 or the following general formula [III]: STR3 wherein Z stands for an oxygen or sulfur atom or a carbonyl or methylene group, R1 stands for a hydrogen or halogen atom or a lower alkyl group or a lower alkoxy group, and n is an integer of from 1 to 5 with the proviso that when n is 2 or more, the groups R1 may be the same or different, and also to processes for the preparation or these ethers of thioethers and a use of these ethers or thioethers. These compounds of the present invention have excellent insecticidal and acaricidal activities while the toxicity of these compounds are very low.
