61638-09-3 Usage
Uses
Used in Research Applications:
2,5-Dimethoxy-4-Methylthiophenylethylamine is used as a research chemical for studying its psychopharmacological effects. It is of interest to scientists due to its potential to provide insights into the mechanisms of action of hallucinogenic drugs and their impact on the human brain.
Used in Recreational Settings:
Despite its potential toxicity and side effects, 2C-T-6 is used recreationally for its psychoactive and hallucinogenic effects. However, it is important to note that the use of this substance is largely considered unsafe for human consumption due to the associated risks.
Used in Pharmaceutical Development:
Although not explicitly mentioned in the provided materials, 2,5-Dimethoxy-4-Methylthiophenylethylamine could potentially be used in the development of new pharmaceuticals, particularly in the field of psychopharmacology. Its effects on the human brain may offer valuable information for the creation of novel treatments for various mental health conditions. However, further research and clinical trials would be necessary to establish its safety and efficacy in such applications.
Check Digit Verification of cas no
The CAS Registry Mumber 61638-09-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,3 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61638-09:
(7*6)+(6*1)+(5*6)+(4*3)+(3*8)+(2*0)+(1*9)=123
123 % 10 = 3
So 61638-09-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H17NO2S/c1-13-9-7-11(15-3)10(14-2)6-8(9)4-5-12/h6-7H,4-5,12H2,1-3H3
61638-09-3Relevant academic research and scientific papers
Sulfur analogs of psychotomimetic amines
Nichols,Shulgin
, p. 1554 - 1556 (2007/10/06)
The syntheses and physical properties are described for 2,5 dimethoxy 4 methylthiophenylethylamine and 2,5 dimethoxy 4 methylthiophenylisopropylamine. The latter compound is the sulfur analog of the psychotomimetic phenylisopropylamines 2,4,5 trimethoxyphenylisopropylamine and 2,5 dimethoxy 4 methylphenylisopropylamine wherein the methylthio group replaces a methoxy group or a methyl group, respectively. This compound is predicted to be about 30 times as active as mescaline.
