817166-24-8 Usage
Uses
Used in Pharmaceutical Industry:
Lepidine, 2-(ethylmercapto)(4CI) is used as a chemical intermediate for the synthesis of new drugs. Its ethyl mercapto group provides a reactive site that can be exploited in the development of pharmaceutical compounds, potentially leading to novel therapeutic agents.
Used in Agricultural Industry:
In the agricultural sector, Lepidine, 2-(ethylmercapto)(4CI) is used as a precursor in the production of pesticides. Its chemical properties make it a suitable candidate for the creation of new agrochemicals that can be used to protect crops from pests and diseases.
Used in Research Laboratories:
Lepidine, 2-(ethylmercapto)(4CI) serves as a versatile building block in organic synthesis within research laboratories. Its unique structure and reactivity are valuable for the development of new materials and compounds, contributing to the advancement of scientific knowledge and potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 817166-24-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,7,1,6 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 817166-24:
(8*8)+(7*1)+(6*7)+(5*1)+(4*6)+(3*6)+(2*2)+(1*4)=168
168 % 10 = 8
So 817166-24-8 is a valid CAS Registry Number.
817166-24-8Relevant academic research and scientific papers
Cu-catalyzed aerobic oxidative cyclizations of 3-N-hydroxyamino-1,2-propadienes with alcohols, thiols, and amines to form α-O-, S-, and N-substituted 4-methylquinoline derivatives
Sharma, Pankaj,Liu, Rai-Shung
, p. 4590 - 4594 (2015/03/18)
A one-pot, two-step synthesis of α-O-, S-, and Nsubstituted 4-methylquinoline derivatives through Cu-catalyzed aerobic oxidations of N-hydroxyaminoallenes with alcohols, thiols, and amines is described. This reaction sequence involves an initial oxidation of N-hydroxyaminoallenes with NuH (Nu = OH, OR, NHR, and SR) to form 3-substituted 2-en-1-ones, followed by Bronsted acid catalyzed intramolecular cyclizations of the resulting products. Our mechanistic analysis suggests that the reactions proceed through a radical-type mechanism rather than a typical ni-trone-intermediate route. The utility of this new Cu-catalyzed reaction is shown by its applicability to the synthesis of several 2-amino-4-methylquinoline derivatives, which are known to be key precursors to several bioactive molecules.
