396129-93-4 Usage
Derivative of amphetamine
1-Piperidineacetic acid, 2-oxo--alpha--phenylis related to the amphetamine class of drugs, which are known for their stimulant effects.
Psychoactive drug
1-Piperidineacetic acid, 2-oxo--alpha--phenyl- has an impact on the central nervous system, altering mental state and producing psychological effects.
Stimulant effects
As a stimulant, it increases energy, alertness, and euphoria in users.
Recreational drug use
The compound is sometimes used for recreational purposes due to its psychoactive properties.
Controlled substance
Due to its potential for abuse and dependence, 1-Piperidineacetic acid, 2-oxo--alpha--phenylis classified as a controlled substance in many jurisdictions.
Health risks
The use of 1-Piperidineacetic acid, 2-oxo--alpha--phenyl- can lead to significant health risks, such as anxiety, paranoia, and cardiovascular problems.
Addictive potential
The compound can be addictive, and长期使用可能导致依赖。
Withdrawal symptoms
Discontinuation of use can result in withdrawal symptoms, which may include physical and psychological discomfort.
Caution and professional supervision
It is important to use 1-Piperidineacetic acid, 2-oxo--alpha--phenylwith caution and under the guidance of a qualified healthcare professional to minimize potential risks and adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 396129-93-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,6,1,2 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 396129-93:
(8*3)+(7*9)+(6*6)+(5*1)+(4*2)+(3*9)+(2*9)+(1*3)=184
184 % 10 = 4
So 396129-93-4 is a valid CAS Registry Number.
396129-93-4Relevant academic research and scientific papers
1,3-Dipolar cycloadditions of new mesoionic compounds. Synthesis of 1H-pyrrolo[1,2-c]thiazoles, pyrrolizines and 5,6,7,8-tetrahydroindolizines
Dalla Croce, Piero,La Rosa, Concetta
, p. 1843 - 1857 (2007/10/03)
We studied the 1,3-dipolar cycloaddition reactions between alkyne dipolarophiles and the new mesoionic compounds 2H,5H,7H-thiazolo[4,3-b]oxazol-2-one (12), 2H,5H,7H-pyrrolo[2,1-b]oxazol-2-one (13) and 2H,5H,7H-oxazolo[3,2-a]pyridin-2-one (14). These 1,3-dipoles were prepared in situ by means of cyclodehydration with acetic anhydride of the corresponding α-substituted 4-oxo-3-thiazolidine- (9), 2-oxo-1-pyrrolidine- (10) and 2-oxo-1-piperidineacetic acids (11). The cycloaddition reactions with alkyne dipolarophiles afforded single 1H-pyrrolo[1,2-c]thiazole, pyrrolizine and 5,6,7,8-tetrahydroindolizine derivatives, or a mixture of the two possible regioisomers, depending on whether symmetrical or unsymmetrical alkynes.
