27563-60-6 Usage
Uses
Used in Pharmaceutical Industry:
2-CYCLOHEXYLACETOHYDRAZIDE is used as an intermediate for the synthesis of various pharmaceuticals, leveraging its ability to inhibit the activity of several enzymes. This makes it a valuable component in the development of drugs targeting specific enzyme-related conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 2-CYCLOHEXYLACETOHYDRAZIDE is utilized as an intermediate in the production of agrochemicals, potentially contributing to the development of new pesticides or herbicides that can effectively control pests and weeds in agriculture.
Used in Anti-Tumor Applications:
2-CYCLOHEXYLACETOHYDRAZIDE is studied for its potential as an anti-tumor agent, indicating its use in oncology research and development for creating therapeutic agents that could combat tumor growth.
Used in Parkinson's Disease Treatment:
2-CYCLOHEXYLACETOHYDRAZIDE is also considered for use in the treatment of Parkinson's disease, as it has shown promise in inhibiting the formation of neurotoxic compounds that contribute to the neurodegenerative aspects of the condition. This application underscores its potential as a therapeutic agent in neurology.
Check Digit Verification of cas no
The CAS Registry Mumber 27563-60-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,5,6 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27563-60:
(7*2)+(6*7)+(5*5)+(4*6)+(3*3)+(2*6)+(1*0)=126
126 % 10 = 6
So 27563-60-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H16N2O/c9-10-8(11)6-7-4-2-1-3-5-7/h7H,1-6,9H2,(H,10,11)
27563-60-6Relevant academic research and scientific papers
NRF2 REGULATORS
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Page/Page column 359, (2017/01/02)
Provided are aryl analogs，pharmaceutical compositions containing them and their use as NRF2 regulators.
Synthesis and SAR evaluation of 1,2,4-triazoles as A2A receptor antagonists
Alanine, Alexander,Anselm, Lilli,Steward, Lucinda,Thomi, Stefan,Vifian, Walter,Groaning, Michael D.
, p. 817 - 821 (2007/10/03)
The synthesis and in vitro structure-activity relationships (SAR) of a series of triazoles as A2A receptor antagonists is reported. This resulted in the identification of potent, selective and permeable 1,2,4-triazoles such as 42 for further op
Acyl hydrazines as precursors to acyl radicals
Braslau, Rebecca,Anderson, Marc O,Rivera, Frank,Jimenez, Armando,Haddad, Terra,Axon, Jonathan R
, p. 5513 - 5523 (2007/10/03)
The use of acyl hydrazines (hydrazides) as precursors for the stoichiometric generation of acyl radicals is explored. Two classes of substrates are examined: unsubstituted acyl hydrazines and acyl hydrazines substituted with a leaving group (2-nitrobenzenesulfonyl or 'nosyl'). Both types are successfully converted to acyl radicals, and are then trapped by nitroxide radicals to give acyloxyamine products. Cyclization reactions are demonstrated for both classes of substrates. A low temperature modification of the McFayden-Stevens reaction is also developed.
