3706-37-4 Usage
Uses
Used in Pharmaceutical Industry:
1-(4-methylphenyl)propan-2-amine hydrochloride (1:1) is used as a psychoactive substance for its stimulant effects on the central nervous system. It is often utilized in the development of medications targeting conditions related to CNS stimulation or as a research compound for studying the effects of stimulants on the brain.
Used in Recreational Drug Market:
1-(4-methylphenyl)propan-2-amine hydrochloride (1:1) is used as a recreational drug due to its psychoactive properties. It is sought after for its stimulating effects and is often sold illicitly under various street names. However, it is important to note that the use of 1-(4-methylphenyl)propan-2-amine hydrochloride (1:1) for recreational purposes is illegal and can pose significant health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 3706-37-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,0 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3706-37:
(6*3)+(5*7)+(4*0)+(3*6)+(2*3)+(1*7)=84
84 % 10 = 4
So 3706-37-4 is a valid CAS Registry Number.
3706-37-4Relevant academic research and scientific papers
Gajda, Tadeusz,Napieraj, Anna,Osowska-Pacewicka, Krystyna,Zawadzki, Stefan,Zwierzak, Andrzej
, p. 4935 - 4946 (1997)
The novel ring-opening reaction of various 2-alkyl- and 2,2-dimethyl-N-(diethoxyphosphoryl)aziridines (1) and (10) with copper-modified Grignard reagents proceeds regiospecifically at the less hindered carbon. The diethyl N-sec-alkylphosphoramidates (2) thus obtained may efficiently be converted to primary sec-alkylamine hydrochlorides (3) by refluxing with 20% hydrochloric acid. 2,3-Disubstituted N-phosphorylated aziridines except N-phosphorylated cyclohexenimine (4) do not react under the described conditions. Copper-mediated reaction of 2-phenyl-N-(diethoxyphosphoryl)aziridine (7) with Grignard reagents affords a mixture of regioisomers (8) and (9) but still with the preference of ring-opening at the carbon of lesser substitution.
