34104-51-3

Basic information

• Product Name: 4-Piperidinol, 4-(4-chlorophenyl)-1-[4-(4-fluorophenyl)-1,4-dioxobutyl]-
• CAS NO: 34104-51-3
• Molecular Formula: C21H21ClFNO3
• Molecular Weight: 389.854
• Mol File: 34104-51-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-Piperidinol, 4-(4-chlorophenyl)-1-[4-(4-fluorophenyl)-1,4-dioxobutyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Piperidinol, 4-(4-chlorophenyl)-1-[4-(4-fluorophenyl)-1,4-dioxobutyl]-(34104-51-3)
• EPA Substance Registry System: 4-Piperidinol, 4-(4-chlorophenyl)-1-[4-(4-fluorophenyl)-1,4-dioxobutyl]-(34104-51-3)

Safety Data

• Hazardous Substances Data: 34104-51-3(Hazardous Substances Data)

Upstream product

• 39512-49-7 4-(4-chlorophenyl)-4-hydroxypiperidine 
• 50536-21-5 C₁₀H₈ClFO₂ 
• 366-77-8 4-(4-fluorophenyl)-4-oxopropionic acid 

Downstream Products

• 34104-67-1 reduced haloperidol 

Relevant articles and documents

Synthesis and binding profile of haloperidol-based bivalent ligands targeting dopamine D2-like receptors

Homodimers of dopamine D2-like receptors are suggested to be of particular importance in the pathophysiology of schizophrenia and, thus, serve as promising targets for the discovery of atypical antipsychotics. This study describes the development of a series of novel bivalent molecules with a pharmacophore derived from the dopamine receptor antagonist haloperidol. These dimers were investigated in comparison to their monomeric analogues for their D2long, D2short, D3, and D4 receptor binding and the ability to bridge two neighboring receptor protomers. Radioligand binding studies provided diagnostic insights when Hill slopes close to two for the bivalent ligand 13 incorporating 22 spacer atoms and a comparative analysis with monovalent control ligands indicated a bivalent binding mode with a simultaneous occupancy of two neighboring binding sites.