518285-55-7 Usage
General Description
(5-Methyl-pyridin-2-yl)-piperidin-4-yl-amine is a chemical compound with potential pharmaceutical applications. It is a combination of a pyridine ring with a piperidine ring, and it contains a methyl group attached to the pyridine ring. (5-Methyl-pyridin-2-yl)-piperidin-4-yl-amine is a type of amine, which is a class of organic compounds that contain a basic nitrogen atom. The specific arrangement of atoms in this compound makes it a potential candidate for drug development, as it may have interactions with biological targets within the body. Further research and testing would be needed to determine the specific properties and potential pharmaceutical uses of this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 518285-55-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,8,2,8 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 518285-55:
(8*5)+(7*1)+(6*8)+(5*2)+(4*8)+(3*5)+(2*5)+(1*5)=167
167 % 10 = 7
So 518285-55-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H17N3/c1-9-2-3-11(13-8-9)14-10-4-6-12-7-5-10/h2-3,8,10,12H,4-7H2,1H3,(H,13,14)
518285-55-7Relevant articles and documents
METHOD FOR MANUFACTURING 4-(5-METHYLPYRIDIN-2-YLAMINO)PIPERIDINE-1-CARBOXYLIC ACID DERIVATIVE
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Page/Page column 5, (2012/06/16)
A novel method for manufacturing 5-methyl-2-(piperidin-4-ylamino)pyridine is established. This method can be used as an industrial manufacturing method to produce a 4-(5-methylpyridin-2-ylamino)piperidine-1-carboxylic acid derivative represented by the general formula, (wherein R represents a linear or branched alkyl group having 1 to 6 carbon atoms or an aralkyl group having 7 to 12 carbon atoms) in a reaction solution having an aromatic monocyclic hydrocarbon as a reaction medium, in the presence of sodium triacetoxyborohydride as a reducing agent, or after adding sodium borohydride and acetic acid to the reaction solution in advance.