90132-18-6

Basic information

• Product Name: Benzaldehyde, 4-ethoxy-3-(ethylthio)-5-methoxy-
• CAS NO: 90132-18-6
• Molecular Formula: C12H16O3S
• Molecular Weight: 240.323
• Mol File: 90132-18-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 4-ethoxy-3-(ethylthio)-5-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 4-ethoxy-3-(ethylthio)-5-methoxy-(90132-18-6)
• EPA Substance Registry System: Benzaldehyde, 4-ethoxy-3-(ethylthio)-5-methoxy-(90132-18-6)

Safety Data

• Hazardous Substances Data: 90132-18-6(Hazardous Substances Data)

Upstream product

• 90245-05-9 [1-(3-Bromo-4-ethoxy-5-methoxy-phenyl)-meth-(E)-ylidene]-cyclohexyl-amine 
• 90109-65-2 3-bromo-4-ethoxy-5-methoxybenzaldehyde 
• 2973-76-4 5-bromo-4-hydroxy-3-methoxybenzaldehyde 

Downstream Products

• 90132-49-3 2-(4-Ethoxy-3-ethylsulfanyl-5-methoxy-phenyl)-ethylamine 
• 90132-45-9 2-[2-(4-Ethoxy-3-ethylsulfanyl-5-methoxy-phenyl)-ethyl]-isoindole-1,3-dione 
• 952017-26-4 2-Ethoxy-1-ethylsulfanyl-5-(2-iodo-ethyl)-3-methoxy-benzene 
• 952017-21-9 2-Ethoxy-1-ethylsulfanyl-3-methoxy-5-vinyl-benzene 
• 90132-29-9 2-Ethoxy-1-ethylsulfanyl-3-methoxy-5-((E)-2-nitro-vinyl)-benzene 

Relevant articles and documents

Sulfur Analogues of Psychotomimetic Agents. 3. Ethyl Homologues of Mescaline and Their Monothio Analogues

All possible monothio analogues of the mono-, di-, and triethoxy homologues of mescaline have been synthesized and pharmacologically evaluated in man.Modifications at the ring position para to the ethylamine chain, either with a sulfur atom, a longer alkyl chain, or both, lead to compounds of high central nervous system activity.The 4-n-propoxy and 4-n-butoxy homologues and their corresponding 4-thio analogues were also synthesized and pharmacologically evaluated.The propyl homologues retain high potency, but a butyl group (either with or without a sulfur atom) leads to a decrease in activity.The m-ethyl or m-thio analogues retain some central action but the diethoxy and especially the triethoxy homologues are relatively inactive as psychotomimetic drugs.