98065-14-6 Usage
General Description
1-(1-phenylpropyl)piperidine, also known as 4'-Methyl-α-pyrrolidinopropiophenone or 4-Methyl-α-PPP, is a chemical compound classified as a stimulant and psychoactive drug. It is a synthetic analog of cathinone, a naturally occurring stimulant found in the khat plant. 1-(1-phenylpropyl)piperidine is a potent psychostimulant that acts on the central nervous system, producing effects similar to those of amphetamines and cocaine. It is commonly used as a recreational drug for its euphoric and stimulant effects, and is considered to have a high potential for abuse and addiction. The substance is also associated with a range of adverse health effects, including cardiovascular and psychiatric problems, and is regulated in many countries.
Check Digit Verification of cas no
The CAS Registry Mumber 98065-14-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,6 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 98065-14:
(7*9)+(6*8)+(5*0)+(4*6)+(3*5)+(2*1)+(1*4)=156
156 % 10 = 6
So 98065-14-6 is a valid CAS Registry Number.
98065-14-6Relevant articles and documents
Atom-efficient transition-metal-free arylation ofN,O-acetals using diarylzinc reagents through Zn/Zn cooperativity
Borys, Andryj M.,Gil-Negrete, Jose M.,Hevia, Eva
, p. 8905 - 8908 (2021/09/10)
Exploiting the cooperative action of Lewis acid Zn(C6F5)2with diarylzinc reagents, the efficient arylation ofN,O-acetals to access diarylmethylamines is reported. Reactions take place under mild reaction conditions without the need for transtion-metal catalysis. Mechanistic investigations have revealed that Zn(C6F5)2not only acts as a Lewis acid activator, but also enables the regeneration of nucleophilic ZnAr2species, allowing a limiting 50 mol% to be employed.
A Synthesis of α-Substituted Amines
Hwang, Yuing C.,Chu, Min,Fowler, Frank W.
, p. 3885 - 3890 (2007/10/02)
The reaction of amides with organolithium reagents followed by hydride reducing agents has been studied as a synthetic route to α-substituted amines.The stereochemistry of the amine has been observed to depend upon the nature of the reducing agent.
