40584-57-4

Basic information

• Product Name: 1-(1-benzothiophen-2-yl)piperidine
• CAS NO: 40584-57-4
• Molecular Formula: C₁₃H₁₅NS
• Molecular Weight: 217.3299
• Mol File: 40584-57-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 363.3°C at 760 mmHg
• Flash Point: 173.5°C
• Density: 1.172g/cm³
• Vapor Pressure: 1.82E-05mmHg at 25°C
• Refractive Index: 1.646
• CAS DataBase Reference: 1-(1-benzothiophen-2-yl)piperidine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1-benzothiophen-2-yl)piperidine(40584-57-4)
• EPA Substance Registry System: 1-(1-benzothiophen-2-yl)piperidine(40584-57-4)

Safety Data

• Hazardous Substances Data: 40584-57-4(Hazardous Substances Data)

Usage

General Description

1-(1-benzothiophen-2-yl)piperidine is a chemical compound with the molecular formula C14H17NS. It is a piperidine derivative with a benzothiophene ring attached to the piperidine nitrogen. 1-(1-benzothiophen-2-yl)piperidine has potential pharmacological properties and may act as a serotonin reuptake inhibitor or an antipsychotic agent. It is also being researched for its potential use in the treatment of mood disorders and schizophrenia. 1-(1-benzothiophen-2-yl)piperidine is a relatively new and emerging compound, and further studies are needed to fully understand its properties and potential applications in the field of medicine and pharmaceuticals.

Upstream product

• 110-89-4 piperidine 
• 5394-13-8 2-bromo-1-benzothiophene 
• 7342-82-7 3-Bromothianaphthene 
• 2142-69-0 2-bromophenyl methyl ketone 
• 5542-49-4 piperidin-1-yl benzoate 
• 95-15-8 Benzo[b]thiophene 

Downstream Products

• 243845-90-1 (4-bromo-phenyl)-(2-piperidin-1-yl-benzo[b]thiophen-3-yl)-methanone 
• 243845-93-4 (4-bromo-phenyl)-[2-(4-methoxy-phenyl)-benzo[b]thiophen-3-yl]-methanone 
• 63676-08-4 2-(4-methoxyphenyl)benzo[b]thiophen-3-yl 4-[2-(1-piperidyl)ethoxy]phenyl ketone 

Relevant articles and documents

Copper(I) iodide-catalyzed synthesis of 1-benzothiophen-2-amines from 4-(2-bromophenyl)-1,2,3-thiadiazole

-

A Convenient Approach to 2-Aminobenzo[b]chalcogenophenes Based on Copper-Catalyzed Transformation of 4-(2-Bromophenyl)-1,2,3-chalcogenodiazoles in the Presence of a Base and Amines

The reactions of 4-(2-bromophenyl)-1,2,3-thia-and -selenadiazoles with amines in the presence of potassium carbonate and copper(I) iodide afforded 2-aminobenzo[b]chalcogenophenes. The corresponding thiaand selenamides, prepared by interaction of 4-(2-brom

Synergistic methodologies for the synthesis of 3-aroyl-2- arylbenzo[b]thiophene-based selective estrogen receptor modulators. Two concise syntheses of raloxifene

Difunctionalized benzo[b]thiophene intermediates are prepared which allow fully independent elaboration of the 2-aryl position or the tether position of benzo[b]thiophene-based selective estrogen receptor modulators (SERMs). Two concise syntheses of the SERM raloxifene (Evista) are presented.