73312-15-9 Usage
Uses
Used in Pharmaceutical Industry:
4-CYANO-4-(3-METHYLPHENYL)CYCLOHEXANONE is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows for the development of novel compounds with potential therapeutic applications, contributing to the advancement of medicine and healthcare.
Used in Agrochemical Industry:
In the agrochemical sector, 4-CYANO-4-(3-METHYLPHENYL)CYCLOHEXANONE serves as an intermediate in the production of agrochemicals. Its incorporation into these products can lead to the creation of innovative solutions for agricultural challenges, such as pest control and crop protection.
Used in Research and Development:
4-CYANO-4-(3-METHYLPHENYL)CYCLOHEXANONE is utilized in research and development for the synthesis of new compounds with potential biological activity. Its presence in the lab allows scientists to explore its properties and reactions, potentially leading to groundbreaking discoveries in the fields of chemistry and biology.
Check Digit Verification of cas no
The CAS Registry Mumber 73312-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,3,1 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73312-15:
(7*7)+(6*3)+(5*3)+(4*1)+(3*2)+(2*1)+(1*5)=99
99 % 10 = 9
So 73312-15-9 is a valid CAS Registry Number.
73312-15-9Relevant academic research and scientific papers
PHARMACEUTICAL COMPOUNDS
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Paragraph 00647; 0650; 0867, (2018/04/26)
This invention relates to compounds that are agonists of the muscarinic M1 receptor or M1 and M4 receptors and which are useful in the treatment of muscarinic M1 or M1/M4 receptor mediated
4-Amino-4-arylcyclohexanones and Their Derivatives, a Novel Class of Analgesics. 1. Modification of the Aryl Ring
Lednicer, Daniel,VonVoigtlander, Philip F.,Emmert, D. Edward
, p. 424 - 430 (2007/10/02)
Investigation of central nervous system activity of phenylcyclohexylamines was continued by preparation of "reversed" analogues.Following the unexpected finding of analgesic activity with 1-(dimethylamino)-1-phenylcyclohexylamine, the SAR of the series was investigated.Synthesis starts by double Michael reaction of acrylate on arylacetonitriles.Following cyclization, decarboxylation, ketalization, and saponification, the geminally substituted acid is rearranged to the isocyanate by means of (C6H5O)2PON3.Isocyanates were then converted to the title compounds.Analgesic activity is very sensitive to the nature and position of the substituent on the aromatic ring.The most potent compounds in this series (p-CH3, p-Br) showed 50percent the potency of morphine.Deletion of the ring oxygen abolishes activity.
