N-Butyryl-N'-cinnamyl-2-methylpiperazine hydrochloride

Base Information

• Chemical Name: N-Butyryl-N'-cinnamyl-2-methylpiperazine hydrochloride
• CAS No.: 98608-59-4
• Molecular Formula: C18H27ClN2O
• Molecular Weight: 322.8728
• UNII: VID4TX8798
• Mol file: 98608-59-4.mol

Synonyms:N-Butyryl-N'-cinnamyl-2-methylpiperazine hydrochloride;98608-59-4;Methyl-ap-237 hydrochloride;VID4TX8798;2-Methyl-1-(1-oxobutyl)-4-(3-phenyl-2-propenyl)piperazine monohydrochloride;1-[2-methyl-4-[(E)-3-phenylprop-2-enyl]piperazin-1-yl]butan-1-one;hydrochloride;Piperazine, 2-methyl-1-(1-oxobutyl)-4-(3-phenyl-2-propenyl)-, monohydrochloride;1-[2-methyl-4-(3-phenyl-2-propen-1-yl)-1-piperazinyl]-1-butanone, monohydrochloride;UNII-VID4TX8798;2-METHYL-AP-237 HYDROCHLORIDE;PD094783;BUCINNAZINE, 2-METHYL HYDROCHLORIDE;LS-112901;1-BUTANONE, 1-(2-METHYL-4-(3-PHENYL-2-PROPEN-1-YL)-1-PIPERAZINYL)-, HYDROCHLORIDE (1:1)

Chemical Property of N-Butyryl-N'-cinnamyl-2-methylpiperazine hydrochloride

Chemical Property:

• Vapor Pressure: 2.77E-08mmHg at 25°C
• Boiling Point: 449.8°Cat760mmHg
• Flash Point: 189.7°C
• Density: g/cm³
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 322.1811912
• Heavy Atom Count: 22
• Complexity: 347

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCC(=O)N1CCN(CC1C)CC=CC2=CC=CC=C2.Cl
• Isomeric SMILES: CCCC(=O)N1CCN(CC1C)C/C=C/C2=CC=CC=C2.Cl
• Use Description: 1-butanoyl-2-methyl-4-[(2E)-3-phenylprop-2-en-1-yl]piperazine hydrochloride is a chemical compound that may have specific applications in the field of pharmacology and drug development. In this context, it could potentially serve as a research compound or intermediate in the synthesis of pharmaceutical agents. Its unique chemical structure suggests it may be involved in studies related to receptor interactions, enzymatic processes, or drug formulation. However, detailed information regarding its specific uses or roles in different fields beyond pharmacology and chemistry is not readily available, indicating that its primary significance lies in drug discovery and related research activities within the pharmaceutical industry.