139891-43-3 Usage
Classification
Stimulant, psychoactive drug
Derivative
Phenmetrazine
Chemical Structure
Similar to amphetamine
Properties
Stimulant: It has stimulant effects on the central nervous system.
Appetite Suppressant: Known to suppress appetite.
Mechanism of Action
Increases levels of neurotransmitters:
Dopamine
Norepinephrine
Effects
Stimulant Effects: Increases alertness and energy.
Appetite Suppression: Decreases feelings of hunger.
Side Effects
Cardiovascular: Increased heart rate, elevated blood pressure.
Psychological: Nervousness, agitation.
Regulatory Status
Controlled Substance: Classified as such in many countries.
Restrictions: Limited use due to potential for abuse and addiction.
Use
Recreational: Has been used recreationally for its stimulant effects.
Note
Similarity to Phenmetrazine: Derived from phenmetrazine, with a comparable structure.
This substance, 2-AMINO-4-PHENYL-BUTYRIC ACID METHYL ESTER or Mephenmetrazine, shares similarities with amphetamine and phenmetrazine. It is classified as a stimulant and has been utilized as a recreational drug. However, its use is associated with side effects such as increased heart rate, elevated blood pressure, and psychological effects like nervousness. Regulatory bodies classify it as a controlled substance due to its potential for abuse and addiction. Its mechanism of action involves increasing levels of neurotransmitters in the brain, including dopamine and norepinephrine, resulting in stimulant and appetite suppressant effects.
Check Digit Verification of cas no
The CAS Registry Mumber 139891-43-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,8,9 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 139891-43:
(8*1)+(7*3)+(6*9)+(5*8)+(4*9)+(3*1)+(2*4)+(1*3)=173
173 % 10 = 3
So 139891-43-3 is a valid CAS Registry Number.
139891-43-3Relevant articles and documents
Controlling diastereoselectivity in the reactions of enantiomerically pure α-bromoacyl-imidazolidinones with nitrogen nucleophiles: Substitution reactions with retention or inversion of configuration
Treweeke,Hitchcock,Pardoe,Caddick
, p. 1868 - 1870 (2007/10/03)
Diastereoselective substitution reactions of α-bromoacyl- imidazolidinones with nitrogen nucleophiles can be promoted with either retention or inversion of configuration by carrying out reactions under epimerising or non-epimerising conditions. The Royal Society of Chemistry 2005.
Catalytic asymmetric Strecker synthesis. Preparation of enantiomerically pure α-amino acid derivatives from aldimines and tributyltin cyanide or achiral aldehydes, amines, and hydrogen cyanide using a chiral zirconium catalyst
Ishitani, Haruro,Komiyama, Susumu,Hasegawa, Yoshiki,Kobayashi, Shu
, p. 762 - 766 (2007/10/03)
Catalytic enantioselective Strecker-type reactions of aldimines with tributyltin cyanide (Bu3SnCN) proceeded smoothly in the presence of a novel chiral zirconium catalyst. High levels of enantioselectivities in the synthesis of α-amino nitrile
