41298-49-1

Basic information

• Product Name: 1-(3-PHENOXYPROPYL)PIPERAZINE
• Synonyms: 1-(3-PHENOXYPROPYL)PIPERAZINE;1-(4-Phenoxypropyl)piperazine;AKOS BC-2677;1-(3-PHENOXYPROPYL)-PIPERAZINE >98%;[3-(Piperazin-1-yl)propoxy]benzene
• CAS NO: 41298-49-1
• Molecular Formula: C₁₃H₂₀N₂O
• Molecular Weight: 220.31
• Product Categories: piperazines
• Mol File: 41298-49-1.mol
• Article Data: 6

Chemical Properties

• Melting Point: 150-152°C
• Boiling Point: 354.6°Cat760mmHg
• Flash Point: 168.2°C
• Appearance: /
• Density: 1.019g/cm³
• Vapor Pressure: 3.32E-05mmHg at 25°C
• Refractive Index: 1.519
• CAS DataBase Reference: 1-(3-PHENOXYPROPYL)PIPERAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-PHENOXYPROPYL)PIPERAZINE(41298-49-1)
• EPA Substance Registry System: 1-(3-PHENOXYPROPYL)PIPERAZINE(41298-49-1)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 41298-49-1(Hazardous Substances Data)

Usage

General Description

1-(3-Phenoxypropyl)piperazine is a chemical compound with the molecular formula C13H20N2O. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 1-(3-PHENOXYPROPYL)PIPERAZINE is a piperazine derivative, which is a class of organic compounds known for their diverse pharmacological activities. Additionally, 1-(3-Phenoxypropyl)piperazine has been studied for its potential antiviral, antipsychotic, and antihistaminic properties. It is also utilized in research and development processes to explore its potential therapeutic applications. However, the compound's specific uses and effects should be carefully evaluated and researched to ensure safety and efficacy.

InChI:InChI=1/C13H20N2O/c1-2-5-13(6-3-1)16-12-4-9-15-10-7-14-8-11-15/h1-3,5-6,14H,4,7-12H2

Upstream product

• 110-85-0 piperazine 
• 588-63-6 3-phenoxypropyl bromide 
• 1384256-96-5 tert-butyl 4-(3-phenoxypropyl)piperazine-1-carboxylate 
• 3384-04-1 3-chloropropyl phenyl ether 

Downstream Products

• 1179874-30-6 8-chloro-11-[4-(3-phenoxypropyl)piperazino]5H-dibenzo[b,e][1,4]diazepine 
• 1384256-86-3 biphenyl-4-yl 3-(4-(3-phenoxypropyl)piperazin-1-yl)acrylate 
• 1383806-58-3 C₁₆H₂₃N₃O 
• 145708-24-3 1-(3-aminopropyl)-4-[3-(phenoxy)propyl]piperazine 
• 138539-94-3 6-[4-(3-phenoxypropyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione.hydrochloride 

Relevant articles and documents

1-Phenoxyalkyl-4-[(N,N-disubstitutedamino)alkyl]piperazine derivatives as non-imidazole histamine H3-antagonists

In this study, a series of 1-phenoxyalkyl-4-[(N,N-disubstitutedamino)alkyl] piperazine derivatives has been prepared and in vitro tested as H 3-receptor antagonists (electrically evoked contraction of the guinea pig jejunum). All compounds inve

Click and photo-unclick chemistry of aminoacrylate for visible light-triggered drug release

"Click and Photo-unclick Chemistry" of aminoacrylates is proposed for a new photo-labile linker. Adducts are built in 2 steps with good yields and cleaved rapidly by tissue penetrable visible light (690 nm) with a photosensitizer. Facile synthesis, release of mother drug, and stability and cleavage in medium are demonstrated.

Synthesis and preliminary pharmacological evaluation of 4′-arylalkyl analogues of clozapine. IV. the effects of aromaticity and isosteric replacement

We report the synthesis and preliminary pharmacological activity of a new series of tricyclic analogues of clozapine as potential antipsychotic agents for the treatment of schizophrenia. These compounds were designed based on a revised structural model, a