50987-66-1

Basic information

• Product Name: 5-(2-CHLOROETHYL)-1,2,3-TRIMETHOXYBENZENE
• Synonyms: 5-(2-CHLOROETHYL)-1,2,3-TRIMETHOXYBENZENE
• CAS NO: 50987-66-1
• Molecular Formula: C₁₁H₁₅ClO₃
• Molecular Weight: 230.69
• Mol File: 50987-66-1.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-(2-CHLOROETHYL)-1,2,3-TRIMETHOXYBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(2-CHLOROETHYL)-1,2,3-TRIMETHOXYBENZENE(50987-66-1)
• EPA Substance Registry System: 5-(2-CHLOROETHYL)-1,2,3-TRIMETHOXYBENZENE(50987-66-1)

Safety Data

• Hazardous Substances Data: 50987-66-1(Hazardous Substances Data)

Upstream product

• 66162-60-5 (3,4,5-trimethoxyphenyl)acetic acid ethyl ester 
• 2989-06-2 methyl 2-(3,4,5-trimethoxyphenyl)acetate 
• 951-82-6 3,4,5-trimethoxyphenyl acetic acid 
• 37785-48-1 2-(3,4,5-trimethoxyphenyl)ethanol 

Downstream Products

• 110513-46-7 O-<2-(3,4,5-Trimethoxyphenyl)-ethyl>-hydroxylamin 
• 113721-17-8 1-<3-(3,4-dichlorophenyl)-3-hydroxypentyl>-4-(3,4,5-trimethoxyphenethyl)piperazine dihydrochloride 
• 71527-52-1 1-methyl-4-<2-(3,4,5-trimethoxyphenyl)ethyl>piperazine 
• 101777-47-3 N-<2-(3,4,5-trimethoxy-phenyl)-aethoxy>-carbamidsaeure-aethylester 
• 71527-50-9 4-(3,4,5-trimethoxy-phenethyl)-morpholine 

Relevant articles and documents

Synthesis and action on the central nervous system of mescaline analogues containing piperazine or homopiperazine rings

Structural juxtaposition of the 3,4,5-trimethoxyphenyl group is the same molecule with a piperazine or homopiperazine ring has been realized in a series of mescaline analogues (I-IV) as part of an investigation into the pharmacological properties of the seven-membered perhydro-1,4-diazepines (homopiperazines). The analogous six-membered piperazines were synthesized and tested as reference substances to determine whether the seven-membered ring conveyed special properties. A variety of pharmacological tests of action on the CNS showed that replacement of the amino group in mescaline by the heterocycles significantly alters the biological activity. In particular, both the piperazine and the homopiperazine derivatives displayed sedative activity to about the same extent.