114366-16-4 Usage
Description
N-(1-METHYLETHYL)-2-PIPERIDINEMETHANAMINE, commonly known as N-methyl-1-phenyl-propan-2-amine, is a synthetic chemical compound belonging to the class of piperidine derivatives. It is closely related to cathinone, a naturally occurring stimulant found in the khat plant, and is known for its stimulant and psychoactive effects.
Uses
Used in Recreational Drug Industry:
N-(1-METHYLETHYL)-2-PIPERIDINEMETHANAMINE is used as a psychostimulant for its euphoric and hallucinogenic effects, often abused for recreational purposes. However, it is classified as a controlled substance in many countries due to its potential for abuse and addiction.
Check Digit Verification of cas no
The CAS Registry Mumber 114366-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,3,6 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 114366-16:
(8*1)+(7*1)+(6*4)+(5*3)+(4*6)+(3*6)+(2*1)+(1*6)=104
104 % 10 = 4
So 114366-16-4 is a valid CAS Registry Number.
114366-16-4Relevant articles and documents
Compounds with Bridgehead Nitrogen 52 -NMR Spectra and Stereochemistry of the 2-Alkylperhydroimidazolopyridines
Banting, Lee,Crabb, Trevor A.
, p. 696 - 706 (2007/10/02)
In contrast to perhydro-oxazolopyridine and perhydrothiazolopyridine, which adopt equilibria in CDCl3 solution at room temperature containing ca 70percent trans-fused conformers in equilibria with O- or S-inside cis-fused conformers, 2-alkylperhydroimidazolopyridines are found to adopt equilibria containing >98percent trans-fused conformers.Comparison of NMR parameters of 2-methylperhydroimidazolopyridine with those of the two isomers of 1,2-dimethylperhydroimidazolopyridine indicates an equilibrium for the former compound between the two trans-fused conformers, with ca 83percent of that conformation containing a transarrangement of nitrogen lone pairs of electrons.These observations are explained in terms of the generalized anomeric effect.KEY WORDS Perhydroimidazolopyridine Conformational equilibria 1H and 13C NMR
