13603-10-6 Usage
Uses
Used in Pharmaceutical Industry:
3-Ethylpiperidine is used as a precursor for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medications. Its unique chemical structure allows for the creation of a wide range of therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Ethylpiperidine is employed as a precursor for the production of various agrochemicals, including pesticides and herbicides. Its role in this industry is crucial for the development of effective and environmentally friendly solutions for crop protection.
Used as a Solvent:
3-Ethylpiperidine is utilized as a solvent in various chemical processes, providing a medium for reactions to occur. Its properties make it suitable for dissolving a wide range of substances, facilitating the synthesis of new compounds.
Used as an Intermediate in Organic Synthesis:
As an intermediate in organic synthesis, 3-Ethylpiperidine plays a vital role in the production of various organic compounds. Its ability to participate in a range of chemical reactions makes it a valuable component in the synthesis of complex organic molecules.
Environmental Considerations:
3-Ethylpiperidine has been identified as a potential environmental contaminant, found in wastewater and soil at low concentrations. It is essential to handle and dispose of 3-Ethylpiperidine properly to prevent environmental pollution and protect human health. Proper management and disposal practices are crucial to mitigate the potential risks associated with 3-Ethylpiperidine.
Check Digit Verification of cas no
The CAS Registry Mumber 13603-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,0 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13603-10:
(7*1)+(6*3)+(5*6)+(4*0)+(3*3)+(2*1)+(1*0)=66
66 % 10 = 6
So 13603-10-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H15N/c1-2-7-4-3-5-8-6-7/h7-8H,2-6H2,1H3
13603-10-6Relevant articles and documents
An approach to the synthesis of 3-substituted piperidines bearing partially fluorinated alkyl groups
Subota, Andrii I.,Ryabukhin, Sergey V.,Gorlova, Alina O.,Grygorenko, Oleksandr O.,Volochnyuk, Dmitriy M.
, p. 61 - 66 (2019/05/29)
An approach to the synthesis of 3-substituted piperidines bearing partially fluorinated alkyl groups was proposed. The method was based on the DAST-mediated nucleophilic fluorination of easily available 2-bromopyridin-3-yl alcohols and ketones affording 2-bromo-3-(1-fluoroalkyl)pyridines and 2-bromo-3-(1,1-difluoroalkyl)pyridines, respectively, followed by catalytic hydrogenation. The hydrogenation step was studied with common heterogeneous Pd-, Pt-, and Rh-based catalyst. It was found that in the case of fluoroalkyl derivatives, the pyridine core reduction was accompanied by hydrodefluorination, which became a limitation of the strategy. Nevertheless, the method worked well with 1,1-difluoroalkyl derivatives
NICOTINIC ACID DERIVATIVES AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS
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Page/Page column 31, (2008/06/13)
The present invention relates to novel nicotinic acid derivatives, of formula (I), wherein the substituents are defined in the specification, their preparation, their use as pharmaceuticals and pharmaceutical compositions containing them.
Novel 3-phenylprop-2-ynylamines as inhibitors of mammalian squalene epoxidase.
Musso, David L,Clarke, Morris J,Kelley, James L,Boswell, G Evan,Chen, Grace
, p. 498 - 506 (2007/10/03)
The synthesis of a novel series of 3-phenylprop-2-ynylamines as selective mammalian squalene epoxidase inhibitors is described. Structure activity relationship studies led to the discovery of compound 19, 1-[3-(3,5-dichlorophenyl)-prop-2-ynyl]-3- methylpiperidine hydrochloride with an IC50 of 2.8 +/- 0.6 microM against rat liver squalene epoxidase. Against 23 strains of fungal squalene epoxidase compound 19 was found to be inactive.
