193686-32-7 Usage
Derivative of piperazine
2,5-Piperazinedione,1-acetyl-3,4-dimethyl-,(S)-(9CI) is derived from piperazine, which is a common structure found in many pharmaceuticals and agrochemicals.
Chiral molecule
2,5-Piperazinedione,1-acetyl-3,4-dimethyl-,(S)-(9CI) exists as a chiral molecule, meaning it has a specific three-dimensional arrangement of atoms that is not superimposable on its mirror image.
(S)-enantiomer
2,5-Piperazinedione,1-acetyl-3,4-dimethyl-,(S)-(9CI) has specific optical properties due to its chirality, and the (S)-enantiomer is specifically noted in the name.
Potential use in the treatment of neurodegenerative diseases
2,5-Piperazinedione,1-acetyl-3,4-dimethyl-,(S)-(9CI) has been studied for its potential therapeutic effects in neurodegenerative diseases, such as Alzheimer's and Parkinson's.
Precursors in the synthesis of biologically active compounds
2,5-Piperazinedione,1-acetyl-3,4-dimethyl-,(S)-(9CI) can be used as a precursor in the synthesis of other biologically active compounds.
Potential health hazards and toxicological effects
This chemical should be handled with care due to its potential health hazards and toxicological effects.
Check Digit Verification of cas no
The CAS Registry Mumber 193686-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,6,8 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 193686-32:
(8*1)+(7*9)+(6*3)+(5*6)+(4*8)+(3*6)+(2*3)+(1*2)=177
177 % 10 = 7
So 193686-32-7 is a valid CAS Registry Number.
193686-32-7Relevant academic research and scientific papers
Selectivity in radical reactions of alanylglycine anhydride derivatives
Chai, Christina L.L.,Hay, Darren B.,King, Alison R.
, p. 605 - 610 (2007/10/03)
Functionalization of N,N′-disubstituted alanylglycine anhydrides under radical conditions is described. The radical (7), generated (i) from reactions of N,N′-disubstituted alanylglycine anhydrides with N-bromosuccinimide, and (ii) from related bromo compounds by reaction with tributyltin deuteride, undergoes carbon-bromine and carbon-deuterium bond formation with moderate to high diastereoselectivities depending on the N-substituents present.
