21168-72-9 Usage
Uses
Used in Pharmaceutical Industry:
2-(4-aminomethyl-piperidin-1-yl)-ethanol is used as a building block in the synthesis of pharmaceuticals for its potential applications in treating various medical conditions. Its unique chemical structure allows it to be incorporated into the development of new drugs and therapeutic agents.
Used in Organic Chemistry:
In the field of organic chemistry, 2-(4-aminomethyl-piperidin-1-yl)-ethanol serves as a valuable reagent in various chemical reactions. Its presence can facilitate the formation of desired products and improve the efficiency of certain synthetic processes.
Used in Chemical Research:
As a reagent in chemical research, 2-(4-aminomethyl-piperidin-1-yl)-ethanol contributes to the advancement of scientific knowledge. It is utilized in experiments and studies to explore its properties, reactivity, and potential applications in different chemical systems.
Used in Nervous System Depressant Studies:
2-(4-aminomethyl-piperidin-1-yl)-ethanol has been studied for its potential as a nervous system depressant. Its effects on the nervous system could lead to the development of new treatments for conditions related to anxiety, stress, and other neurological disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 21168-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,1,6 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21168-72:
(7*2)+(6*1)+(5*1)+(4*6)+(3*8)+(2*7)+(1*2)=89
89 % 10 = 9
So 21168-72-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H18N2O/c9-7-8-1-3-10(4-2-8)5-6-11/h8,11H,1-7,9H2
21168-72-9Relevant academic research and scientific papers
A 1-substituted piperidine derivatives method for the preparation of
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Paragraph 0022; 0023, (2018/02/04)
The invention discloses a preparation method of one-bit-substituted piperidine derivative, i.e., 2-(4-((ethyl-amino)methyl)piperidine-1-radical)alcohol. The preparation method adopts piperidine-4-formamide as a starting material, and obtains a target product by substitution reaction, reduction reaction and substitution reaction. The compound is an important medical intermediate.
Substituted imidazo[1,2-b]pyridazines as protein kinase inhibitors
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Page/Page column 143; 144, (2016/09/13)
The present invention provides protein kinase having one of the following structures (I), (II) or (III): or a stereoisomer, prodrug, tautomer or pharmaceutically acceptable salt thereof, wherein R, R1, R2 and X are as defined herein. Compositions and methods for using the same in the treatment of cancer, autoimmune, inflammatory and other Pim kinase-associated conditions are also disclosed.
HETEROCYCLIC PROTEIN KINASE INHIBITORS
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Paragraph 00349; 00350, (2013/03/26)
The present invention provides protein kinase having one of the following structures (I), (II) or (III): or a stereoisomer, prodrug, tautomer or pharmaceutically acceptable salt thereof, wherein R, R1, R2 and X are as defined herein. Compositions and methods for using the same in the treatment of cancer, autoimmune, inflammatory and other Pim kinase-associated conditions are also disclosed.
