90943-48-9

Basic information

• Product Name: 1-(3-chloropropoxy)-2-methoxybenzene
• Synonyms: 1-(3-chloropropoxy)-2-methoxybenzene
• CAS NO: 90943-48-9
• Molecular Weight: 200.665
• Mol File: 90943-48-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(3-chloropropoxy)-2-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-chloropropoxy)-2-methoxybenzene(90943-48-9)
• EPA Substance Registry System: 1-(3-chloropropoxy)-2-methoxybenzene(90943-48-9)

Safety Data

• Hazardous Substances Data: 90943-48-9(Hazardous Substances Data)

Upstream product

• 90-05-1 2-methoxy-phenol 
• 109-70-6 1.3-chlorobromopropane 

Downstream Products

• 1364171-44-7 1-(4-chlorobenzyl)-4-(3-(2-methoxyphenoxy)propyl)piperazine 
• 1364171-42-5 1-(2-chlorobenzyl)-4-(3-(2-methoxyphenoxy)propyl)piperazine 
• 1042712-01-5 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinecarboxylic acid methyl ester 2-(N-4-(3-(2-methoxyphenoxy)propyl)piperazinyl)ethyl ester 
• 111626-14-3 α,α-bis(4-fluorophenyl)-1-[3-(2-methoxyphenoxy)propyl]-4-piperidinemethanol 
• 111626-13-2 4-[bis(4-fluorophenyl)methyl]-1-[3-(2-methoxyphenoxy)propyl]piperidine 

Relevant articles and documents

Synthesis and computational studies on aryloxypropyl piperazine derivatives as potential atypical antipsychotic agents

A series of aryloxypropyl derivatives have been synthesized and evaluated for atypical antipsychotic activity in apomorphine induced mesh climbing and stereotypy assays in mice and the compounds displayed good efficacy coupled with an atypical profile. In

Synthesis and Antiallergy Activity of 4-(Diarylhydroxymethyl)-1-piperidines and Structurally Related Compounds

A series of 4-(diarylhydroxymethyl)-1-piperidines was synthesized and evaluated for antiallergy activity.Several analogues had potent activity in the passive foot anaphylaxis (PFA) assay, an IgE-mediated model useful in the detection of compounds possessing antiallergic activity.In particular 1--1-piperidinyl>propoxy>-3-methoxyphenyl>ethanone (1, AHR-5333) was more potent than oxatomide and terfenadine in this assay.