114366-10-8 Usage
Uses
Used in Pharmaceutical Industry:
2-Pyridinemethanamine,5-ethyl-N-methyl-(9CI) is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, including the pyridine ring and the attached ethyl and methyl groups, may contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Pyridinemethanamine,5-ethyl-N-methyl-(9CI) may serve as a precursor for the production of pesticides or other agrochemicals. Its nitrogen-containing structure could be utilized to create compounds with pesticidal or herbicidal activity, potentially enhancing crop protection and yield.
Used in Research and Development:
2-Pyridinemethanamine,5-ethyl-N-methyl-(9CI) is used as a research compound for studying its chemical properties, reactivity, and potential applications in various fields. Scientists and researchers may explore its interactions with other molecules, its ability to form complexes, or its use in the development of new materials or processes.
Check Digit Verification of cas no
The CAS Registry Mumber 114366-10-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,3,6 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 114366-10:
(8*1)+(7*1)+(6*4)+(5*3)+(4*6)+(3*6)+(2*1)+(1*0)=98
98 % 10 = 8
So 114366-10-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H14N2/c1-3-8-4-5-9(7-10-2)11-6-8/h4-6,10H,3,7H2,1-2H3
114366-10-8Relevant academic research and scientific papers
Compounds with Bridgehead Nitrogen 52 -NMR Spectra and Stereochemistry of the 2-Alkylperhydroimidazolopyridines
Banting, Lee,Crabb, Trevor A.
, p. 696 - 706 (2007/10/02)
In contrast to perhydro-oxazolopyridine and perhydrothiazolopyridine, which adopt equilibria in CDCl3 solution at room temperature containing ca 70percent trans-fused conformers in equilibria with O- or S-inside cis-fused conformers, 2-alkylperhydroimidazolopyridines are found to adopt equilibria containing >98percent trans-fused conformers.Comparison of NMR parameters of 2-methylperhydroimidazolopyridine with those of the two isomers of 1,2-dimethylperhydroimidazolopyridine indicates an equilibrium for the former compound between the two trans-fused conformers, with ca 83percent of that conformation containing a transarrangement of nitrogen lone pairs of electrons.These observations are explained in terms of the generalized anomeric effect.KEY WORDS Perhydroimidazolopyridine Conformational equilibria 1H and 13C NMR
