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228418-82-4

228418-82-4 Structure

228418-82-4 Structure
IdentificationBack Directory
[Name]

(S)-1-CYCLOHEXYL-4-[4-(2-METHOXY-PHENYL)-PIPERAZIN-1-YL]-2-PHENYL-BUTAN-1-ONE
[CAS]

228418-82-4
[Synonyms]

LY426965, S-(+)-
(S)-1-CYCLOHEXYL-4-[4-(2-METHOXY-PHENYL)-PIPERAZIN-1-YL]-2-PHENYL-BUTAN-1-ONE
(S)-1-Cyclohexyl-4-(4-(2-methoxyphenyl)piperazin-1-yl)-2-methyl-2-phenylbutan-1-one
1-BUTANONE, 1-CYCLOHEXYL-4-[4-(2-METHOXYPHENYL)-1-PIPERAZINYL]-2-METHYL-2-PHENYL-, (2S)-
1-CYCLOHEXYL-4-[4-(2-METHOXYPHENYL)-1-PIPERAZINYL]-2-METHYL-2-PHENYL-1-BUTANONE, (S)-(+)-
[Molecular Formula]

C28H38N2O2
[MDL Number]

MFCD10565913
[MOL File]

228418-82-4.mol
[Molecular Weight]

434.61
Chemical PropertiesBack Directory
[Boiling point ]

587.8±50.0 °C(Predicted)
[density ]

1.082±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

7.17±0.10(Predicted)
Safety DataBack Directory
[HS Code ]

2933599590
Hazard InformationBack Directory
[Uses]

LY426965 is a potent arylpiperazine compound known for its role as a full antagonist of the serotonin 1A receptor, lacking partial agonist activity. It is identified as a selective 5-HT1A antagonist, showing promise in preclinical studies for treating conditions associated with serotonin dysregulation, such as smoking cessation and depression-related disorders[1].
[References]

[1] Asymmetric Construction of Quaternary Centers by Enantioselective Allylation: Application to the Synthesis of the Serotonin Antagonist LY426965
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