54419-64-6 Usage
Description
2-5-dimethoxybutyrophenone, a synthetic phenethylamine derivative, is a member of the butyrophenone class of compounds. With the chemical formula C13H18O3, it is related to psychoactive compounds such as MDMA and MDA. Known for its hallucinogenic effects when ingested, this potent serotonin receptor agonist has been utilized in research studies to explore its impact on the central nervous system. Due to its potential for abuse and hallucinogenic properties, it is classified as a controlled substance in many countries.
Uses
Used in Research Studies:
2-5-dimethoxybutyrophenone is used as a research chemical for investigating its effects on the central nervous system. It aids scientists in understanding the mechanisms of action and potential applications related to its psychoactive properties.
Used in Psychopharmacology:
In the field of psychopharmacology, 2-5-dimethoxybutyrophenone is used as a potent serotonin receptor agonist. This application is crucial for studying the interactions between the compound and the serotonin receptors, which can provide insights into the development of new therapeutic agents for various neurological and psychiatric disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 54419-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,1 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54419-64:
(7*5)+(6*4)+(5*4)+(4*1)+(3*9)+(2*6)+(1*4)=126
126 % 10 = 6
So 54419-64-6 is a valid CAS Registry Number.
54419-64-6Relevant articles and documents
Pyrazolyl-Based Carboxamides II
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Paragraph 0567-0569, (2014/07/22)
The invention relates to pyrazolyl-based carboxamide compounds useful as ICRAC inhibitors, to pharmaceutical compositions containing these compounds and to these compounds for the use in the treatment and/or prophylaxis of diseases and/or disorders, in particular inflammatory diseases and/or inflammatory disorders.
The Chemistry of Nitrilium Salts. Part 1. Acylation of Phenols and Phenol Ethers with Nitriles and Trifluoromethanesulphonic Acid
Booth, Brian L.,Noori, Ghazi F.M.
, p. 2894 - 2900 (2007/10/02)
Aliphatic nitriles, RCN (R = Me, n-Pr, CH2Cl, and CCl3), in the presence of trifluoromethanesulphonic acid have been found to react with a number of mono-, di-, and tri-substituted phenols and phenol ethers at room temperature to give ketones after hydrolysis of the reaction mixture.Moderate to good yields of acylation products are obtained in the majority of these reactions.The yield with malononitrile and succinonitrile, which are only slightly soluble in the reaction medium, are generally poor, and reaction involves only one of the available nitrile groups.Attempts to use diethyl ether and dichloromethane as solvents for some of these reactions were unsuccessful, but limited success was achieved with nitromethane.
Studies on dimethoxyphenylaminoalcohols. II. Syntheses and relative configulations of 1 dimethoxyphenyl 3 (alkylamino)butanols
Hamano,Okuda
, p. 1348 - 1359 (2007/10/05)
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