3568-94-3 Usage
Description
4-Methylaminorex is a stimulant drug belonging to the 2-amino-5-aryloxazoline class. It exhibits effects similar to Methamphetamine but with a significantly longer duration. This substance is known for its stimulant properties, which include inducing euphoria, enhancing attention, and improving cognitive functions.
Uses
Used in Research and Development:
4-Methylaminorex is used as a research compound for studying the effects of stimulant drugs on the human body. Its long-lasting effects make it a valuable tool for understanding the mechanisms behind stimulant-induced euphoria, attention, and cognition enhancement.
Used in Controlled Substances Regulation:
As a controlled substance, 4-Methylaminorex is used in the development and enforcement of regulations and policies related to the control and monitoring of stimulant drugs. This helps in preventing the misuse and abuse of such substances, ensuring public health and safety.
Please note that the use of 4-Methylaminorex for any purpose other than research and controlled substances regulation is not recommended due to its potential for abuse and health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 3568-94-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,6 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3568-94:
(6*3)+(5*5)+(4*6)+(3*8)+(2*9)+(1*4)=113
113 % 10 = 3
So 3568-94-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O/c1-7-9(13-10(11)12-7)8-5-3-2-4-6-8/h2-7,9H,1H3,(H2,11,12)/t7-,9-/m1/s1
3568-94-3Relevant articles and documents
Regioselective Formal [3+2] Cycloadditions of Urea Substrates with Activated and Unactivated Olefins for Intermolecular Olefin Aminooxygenation
Wu, Fan,Alom, Nur-E,Ariyarathna, Jeewani P.,Na?, Johannes,Li, Wei
supporting information, p. 11676 - 11680 (2019/07/31)
A new class of intermolecular olefin aminooxygenation reaction is described. This reaction utilizes the classic halonium intermediate as a regio- and stereochemical template to accomplish the selective oxyamination of both activated and unactivated alkenes. Notably, urea chemical feedstock can be directly introduced as the N and O source and a simple iodide salt can be utilized as the catalyst. This formal [3+2] cycloaddition process provides a highly modular entry to a range of useful heterocyclic products with excellent selectivity and functional-group tolerance.
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