1010385-24-6 Usage
General Description
(1S)-1-(3-Methoxyphenyl)pentylamine, also known as 3-MeO-α-ET, is a chemical compound that belongs to the class of substituted phenethylamines. It is a psychoactive drug and is commonly used for recreational purposes due to its stimulating and psychedelic effects. The compound acts as a serotonin and norepinephrine releasing agent and also has affinity for serotonin and dopamine receptors. It is reported to produce feelings of empathy, euphoria, and heightened sensory perception in users. However, it is important to note that the use of this compound can also have potential negative effects such as increased blood pressure, heart rate, and body temperature, as well as potential neurotoxicity. Therefore, caution should be exercised when using (1S)-1-(3-Methoxyphenyl)pentylamine.
Check Digit Verification of cas no
The CAS Registry Mumber 1010385-24-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,0,3,8 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1010385-24:
(9*1)+(8*0)+(7*1)+(6*0)+(5*3)+(4*8)+(3*5)+(2*2)+(1*4)=86
86 % 10 = 6
So 1010385-24-6 is a valid CAS Registry Number.
1010385-24-6Relevant articles and documents
Alternative and complementary approaches to the asymmetric synthesis of C3 substituted NH free or N-substituted isoindolin-1-ones
Lamblin, Marc,Couture, Axel,Deniau, Eric,Grandclaudon, Pierre
, p. 111 - 123 (2008/09/17)
Complementary synthetic approaches to enantiomerically pure C3 alkylated or arylated NH free or N-substituted isoindolinones have been developed. The key step is elaboration of diversely substituted 2-alkyl- and arylbenzylamines, which can be submitted to a bis-metallation process followed by interception with a carbonylating agent. They can be also converted into N-alkylbromobenzylcarbamates or into bromobenzyldicarbamates and the assembly of the titled compounds can be readily ensured by reliance upon the Parham cyclization process.
