For research use only. Not for therapeutic Use.
N-Boc-N-desmethyl Zopiclone-d8 is a deuterated derivative of N-desmethyl Zopiclone, where eight hydrogen atoms are replaced with deuterium. This compound is protected with a Boc (tert-butoxycarbonyl) group, commonly used in organic synthesis and pharmaceutical research. The deuterium labeling makes this compound particularly useful for studying the pharmacokinetics, metabolism, and degradation pathways of Zopiclone analogs using mass spectrometry. N-Boc-N-desmethyl Zopiclone-d8 is instrumental in research focused on optimizing sedative-hypnotic drugs, allowing researchers to track and analyze the behavior of the compound with high precision, thereby contributing to the development of safer and more effective treatments for sleep disorders.
Catalog Number | R013830 |
CAS Number | 1246820-47-2 |
Synonyms | 1-tert-Butyl 4-[6-(5-Chloropyridin-2-yl)-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-5-yl]piperazine-1,4-dicarboxylate-d8; 1,4-Piperazinedicarboxylic Acid 1-[6-(5-Chloro-2-pyridinyl)-6,7-dihydro-7-oxo-5H-pyrrolo[3,4-b]pyrazin-5-yl] 4-(1,1-Dimethylethy |
Molecular Formula | C21H23ClN6O5 |
Purity | ≥95% |
Storage | Room temperature |
IUPAC Name | 4-O-tert-butyl 1-O-[6-(5-chloropyridin-2-yl)-5-oxo-7H-pyrrolo[3,4-b]pyrazin-7-yl] 2,2,3,3,5,5,6,6-octadeuteriopiperazine-1,4-dicarboxylate |
InChI | InChI=1S/C21H23ClN6O5/c1-21(2,3)33-20(31)27-10-8-26(9-11-27)19(30)32-18-16-15(23-6-7-24-16)17(29)28(18)14-5-4-13(22)12-25-14/h4-7,12,18H,8-11H2,1-3H3/i8D2,9D2,10D2,11D2 |
InChIKey | WCXISODDJDGVCJ-JNJBWJDISA-N |
SMILES | [2H]C1(C(N(C(C(N1C(=O)OC2C3=NC=CN=C3C(=O)N2C4=NC=C(C=C4)Cl)([2H])[2H])([2H])[2H])C(=O)OC(C)(C)C)([2H])[2H])[2H] |