3166-74-3 Usage
Description
2,5-Dimethoxyphenethylamine hydrochloride, also known as 2C-H, is a psychoactive substance belonging to the 2,5-phenethylamine class, commonly referred to as 2Cs. It is characterized by its ability to activate the 5-HT2C receptor to a lesser extent than serotonin, with a pEC50 value of 5.93. Unlike the 4-substituted 2C forms, 2C-H has little effect on serotonin receptors. This product is primarily intended for research and forensic applications.
Uses
Used in Research Applications:
2,5-Dimethoxyphenethylamine hydrochloride is used as a research chemical for studying the effects of psychoactive substances on the central nervous system and their interactions with serotonin receptors. Its selective activation of the 5-HT2C receptor makes it a valuable tool in understanding the mechanisms of action and potential therapeutic applications of related compounds.
Used in Forensic Applications:
In forensic science, 2,5-Dimethoxyphenethylamine hydrochloride is utilized for the identification and analysis of controlled substances in criminal investigations. Its unique chemical properties and psychoactive effects make it a target for forensic analysis in cases involving the abuse or trafficking of designer drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 3166-74-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,6 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3166-74:
(6*3)+(5*1)+(4*6)+(3*6)+(2*7)+(1*4)=83
83 % 10 = 3
So 3166-74-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO2/c1-12-9-3-4-10(13-2)8(7-9)5-6-11/h3-4,7H,5-6,11H2,1-2H3
3166-74-3Relevant articles and documents
Synthesis of deuterium labeled phenethylamine derivatives
Xu, Ya-Zhu,Chen, Chinpiao
, p. 1187 - 1200 (2008/04/18)
The synthesis of a series of five deuterium labeled phenethylamine derivatives, 4-bromo-2,5-[2H6]-dimethoxyphenethylamine (2C-B), 4-chloro-2,5-[2H6]-dimethoxyphenethylamine (2C-C), 2,5-[2H6]-dimethoxy-4-iodophenethylamine (2C-I), 2,5-[2H6]-dimethoxy-4-ethylthiophenethylamine (2C-T-2) and 2,5-[2H6]-dimethoxy-4-n-propylthiophenethylamine (2C-T-7) from 1,4-[2H6]-dimethoxybenzene is described. The isotopically labeled compounds are used as internal standards in gas chromatography-mass spectrometry (GC-MS) assays. Copyright
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