793675-05-5 Usage
General Description
(5-Methyl-pyridin-2-yl)-piperidin-4-yl-amine dihydrochloride is a chemical compound that consists of a piperidine ring and a pyridine ring, along with an amine group. It is typically found in the form of a dihydrochloride salt. This chemical has potential applications in the field of pharmaceuticals and organic synthesis due to its unique structural properties. It may be used as a building block in the synthesis of various organic compounds, and it may also have biological activity that could make it useful in drug discovery and development. Additionally, its dihydrochloride salt form enhances its solubility in water, which can be advantageous for certain applications. Further research and studies may be needed to fully understand the potential uses and properties of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 793675-05-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,3,6,7 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 793675-05:
(8*7)+(7*9)+(6*3)+(5*6)+(4*7)+(3*5)+(2*0)+(1*5)=215
215 % 10 = 5
So 793675-05-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H17N3.2ClH/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);2*1H
793675-05-5Relevant articles and documents
METHOD FOR MANUFACTURING 4-(5-METHYLPYRIDIN-2-YLAMINO)PIPERIDINE-1-CARBOXYLIC ACID DERIVATIVE
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Page/Page column 6-7, (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.
