45584-07-4 Usage
General Description
4-Amino-1-methylpiperidine is a chemical compound with the molecular formula C6H14N2. It is a piperidine derivative that consists of a piperidine ring with a methyl group attached to the nitrogen atom and an amino group attached to the carbon atom in the 4 position. This chemical is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a building block in the production of various drugs and active pharmaceutical ingredients. Additionally, it has potential applications in research and development for the synthesis of novel compounds with biological activity. Overall, 4-amino-1-methylpiperidine is a versatile chemical with important industrial and scientific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 45584-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,5,8 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 45584-07:
(7*4)+(6*5)+(5*5)+(4*8)+(3*4)+(2*0)+(1*7)=134
134 % 10 = 4
So 45584-07-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2/c1-7-6-2-4-8-5-3-6/h6-8H,2-5H2,1H3
45584-07-4Relevant articles and documents
The effect of substitution on the utility of piperidines and octahydroindoles for reversible hydrogen storage
Cui, Yi,Kwok, Samantha,Bucholtz, Andrew,Davis, Boyd,Whitney, Ralph A.,Jessop, Philip G.
, p. 1027 - 1037 (2008/12/20)
Substituted piperidines and octahydroindoles are compared in terms of their usability as reversible organic hydrogen storage liquids for hydrogen-powered fuel cells. Theoretical Gaussian calculations indicate which structural features are likely to lower the enthalpy of dehydrogenation. Experimental results show that attaching electron donating or conjugated substituents to the piperidine ring greatly increases the rate of catalytic dehydrogenation, with the greatest rates being observed with 4-aminopiperidine and piperidine-4-carboxamide. Undesired side reactions were observed with some compounds such as alkyl transfer reactions during the dehydrogenation of 4-dimethylaminopiperidine, C-O and C-N cleavage reactions during hydrogenation and/or subsequent dehydrogenation of 4-alkoxy and 4-amino indoles, and disproportionation during the hydrogenation of 4-aminopyridine. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.
