138680-08-7

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138680-08-7 Structure

Identification	Back Directory
[Name] (R)-Zopiclone
[CAS] 138680-08-7
[Synonyms] (R)-zolpiclone Zopiclone R-Isomer Zopiclone Impurity 4 ((R)-Zopiclone) 5H-Pyrrolo[3,4-b]pyrazine, 1-piperazinecarboxylic acid deriv. [(7R)-6-(5-chloropyridin-2-yl)-5-oxo-7H-pyrrolo[3,4-b]pyrazin-7-yl] 4-methylpiperazine-1-carboxylate (R)-6-(5-chloropyridin-2-yl)-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-5-yl4-methylpiperazine-1-carboxylate (R)-4-Methyl-6-(5-chloro-2-pyridinyl)-6,7-dihydro-7-oxo-5H-pyrrolo[3,4-b]pyrazin-5-yl-1-piperazinecarboxylic Acid 4-Methyl-6-(5-chloro-2-pyridinyl)-6,7-dihydro-7-oxo-5H-pyrrolo(3,4-b)pyrazin-5-yl ester-1-Piperazinecarboxylic acid 1-Piperazinecarboxylic acid, 4-methyl-, (5R)-6-(5-chloro-2-pyridinyl)-6,7-dihydro-7-oxo-5H-pyrrolo[3,4-b]pyrazin-5-yl ester 1-Piperazinecarboxylic acid, 4-methyl-, 6-(5-chloro-2-pyridinyl)-6,7-dihydro-7-oxo-5H-pyrrolo[3,4-b]pyrazin-5-yl ester, (R)- 1-Piperazinecarboxylic acid, 4-methyl-, (5R)-6-(5-chloro-2-pyridinyl)-6,7-dihydro-7-oxo-5H-pyrrolo[3,4-b]pyrazin-5-yl ester (9CI) Zopiclone R-Isomer CIV (10 mg) ((-)-(5R)-6-(5-Chloropyridin-2-yl)-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-5-yl 4-methylpiperazine-1-carboxylate)
[Molecular Formula] C17H17ClN6O3
[MOL File] 138680-08-7.mol
[Molecular Weight] 388.81

Chemical Properties	Back Directory
[Boiling point ] 580.7±50.0 °C(Predicted)
[density ] 1.54±0.1 g/cm3(Predicted)
[storage temp. ] -10 to -25°C
[solubility ] DMSO (Slightly), Methanol (Slightly)
[form ] Solid
[pka] 6.70±0.10(Predicted)
[color ] White to Pale Yellow
[Stability:] Stable under recommended storage conditions., Stable Under Recommended Storage C

Safety Data	Back Directory
[HS Code ] 2933790002

Hazard Information	Back Directory
[Uses] (R)-Zopiclone is the (R)-enantiomer of Zopiclone (Z700500). (R)-Zopiclone is known to have sedative and anxiolytic effects and as well as effects towards locomotor activity reduction.
[Definition] ChEBI: (5R)-zopiclone is the (5R)-enantiomer of zopiclone. It is an enantiomer of an eszopiclone.

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