59573-44-3 Usage
Uses
Used in Pharmaceutical Industry:
(+)-(2S,5S)-2,5-dimethylpiperazine serves as a crucial building block in the synthesis of various pharmaceuticals. Its unique stereochemistry and molecular structure contribute to the development of drugs with specific therapeutic effects and reduced side effects, enhancing the overall efficacy and safety of medications.
Used in Organic Synthesis:
In the field of organic synthesis, (+)-(2S,5S)-2,5-dimethylpiperazine is utilized as a versatile intermediate for the creation of a broad range of organic compounds. Its ability to form stable derivatives and participate in various chemical reactions makes it an indispensable component in the synthesis of complex organic molecules for research and industrial purposes.
Used in Research and Development:
(+)-(2S,5S)-2,5-dimethylpiperazine plays a significant role in research and development, particularly in the study of stereochemistry, drug discovery, and the development of novel chemical entities. Its unique properties allow scientists to explore new avenues in chemical and pharmaceutical research, leading to advancements in various scientific disciplines.
Check Digit Verification of cas no
The CAS Registry Mumber 59573-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,7 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59573-44:
(7*5)+(6*9)+(5*5)+(4*7)+(3*3)+(2*4)+(1*4)=163
163 % 10 = 3
So 59573-44-3 is a valid CAS Registry Number.
59573-44-3Relevant academic research and scientific papers
Reversible Interconversion between 2,5-Dimethylpyrazine and 2,5-Dimethylpiperazine by Iridium-Catalyzed Hydrogenation/Dehydrogenation for Efficient Hydrogen Storage
Fujita, Ken-Ichi,Wada, Tomokatsu,Shiraishi, Takumi
supporting information, p. 10886 - 10889 (2017/08/30)
A new hydrogen storage system based on the hydrogenation and dehydrogenation of nitrogen heterocyclic compounds, employing a single iridium catalyst, has been developed. Efficient hydrogen storage using relatively small amounts of solvent compared with previous systems was achieved by this new system. Reversible transformations between 2,5-dimethylpyrazine and 2,5-dimethylpiperazine, accompanied by the uptake and release of three equivalents of hydrogen, could be repeated almost quantitatively at least four times without any loss of efficiency. Furthermore, hydrogen storage under solvent-free conditions was also accomplished.
Process for preparing Cis-2,6-dimethylpiperazine
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Example 2, (2008/06/13)
This invention relates to a process for the selective preparation of cis-2,6-dimethylpiperazine by reacting (i) a diisopropanolamine mixture comprising compounds having the formulas HN(CH2CH(OH)CH3)2, HN(CH(CH3)CH2OH)2, and HN(CH(CH3)CH2OH)(CH2CH(OH)CH3) or (ii) 1,2-diaminopropane with ammonia and hydrogen in the presence of a hydrogenation catalyst.
