7404-67-3 Usage
Uses
Given the nature of MTMP as described, it does not have approved therapeutic uses due to its high potential for abuse and associated health risks. However, in a hypothetical scenario where it might be considered for research purposes, it could be used as follows:
Used in Pharmaceutical Research:
METHYL-THIOPHEN-2-YLMETHYL-AMINE HYDROCHLORIDE could be utilized as a research chemical for studying the effects of psychoactive substances on the central nervous system and their potential applications in the development of new medications for various disorders. This would be for understanding the mechanisms of action and side effects associated with this class of compounds.
Used in Forensic Toxicology:
In the field of forensic toxicology, METHYL-THIOPHEN-2-YLMETHYL-AMINE HYDROCHLORIDE could be employed as a reference substance for identifying and analyzing the presence of synthetic stimulants in biological samples, which is crucial for cases involving substance abuse or poisoning.
Check Digit Verification of cas no
The CAS Registry Mumber 7404-67-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7404-67:
(6*7)+(5*4)+(4*0)+(3*4)+(2*6)+(1*7)=93
93 % 10 = 3
So 7404-67-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NS.ClH/c1-7-5-6-3-2-4-8-6;/h2-4,7H,5H2,1H3;1H
7404-67-3Relevant academic research and scientific papers
Selective synthesis of mono- and di-methylated amines using methanol and sodium azide as C1 and N1 sources
Chakrabarti, Kaushik,Mishra, Anju,Panja, Dibyajyoti,Paul, Bhaskar,Kundu, Sabuj
supporting information, p. 3339 - 3345 (2018/07/29)
A Ru(ii) complex mediated synthesis of various N,N-dimethyl and N-monomethyl amines from organic azides using methanol as a methylating agent is reported. This methodology was successfully applied for a one-pot reaction of bromide derivatives and sodium azide in methanol. Notably, by controlling the reaction time several N-monomethylated and N,N-dimethylated amines were synthesized selectively. The practical applicability of this tandem process was revealed by preparative scale reactions with different organic azides and synthesis of an anti-vertigo drug betahistine. Several kinetic experiments and DFT studies were carried out to understand the mechanism of this transformation.
