19679-59-5

Usage

Type of substance

Stimulant and appetite suppressant

Former use

Prescription medication for the treatment of obesity

Discontinuation reason

Potential for abuse and addiction

Mechanism of action

Stimulates the release of certain neurotransmitters in the brain

Effects

Increased energy and decreased appetite

Side effects

Increased heart rate, high blood pressure, potential damage to the heart and blood vessels

Legal status

Schedule IV controlled substance by the United Nations

Legal restrictions

Illegal to manufacture, distribute, or possess without a license

Upstream product

• 57-14-7 N,N-Dimethylhydrazine 
• 93-55-0 1-phenyl-propan-1-one 

Downstream Products

• 107112-64-1 N,N-dimethylhydrazone de methyl-2 phenyl-1 (tetrahydropyrannyle ether)-6 hexanone 
• 107112-65-2 N,N-dimethylhydrazone de methyl-2 phenyl-1 (tetrahydropyrannyle ether)-6 hexanone 
• 92898-27-6 2,4-dimethyl-2-pent-4-enyl-3,5-diphenyl-2H-pyrrole 
• 88453-93-4 (triphenylcyclopropenyl)-propiophenone N,N-dimethylhydrazone 
• 110775-38-7 1-phenyl-5-hexenyl-1-amine 
• 110775-35-4 3,4-dimethyl-2-pent-4-enyl-2,5-diphenyl-2H-pyrrole 
• 109925-99-7 1-phenylpent-4-enylamine 
• 110775-33-2 2-but-3-enyl-3,4-dimethyl-2,5-diphenyl-2H-pyrrole 
• 93-55-0 1-phenyl-propan-1-one 
• 110775-55-8 Z-2-methyl-1-phenylhept-6-en-1-one dimethylhdrazone 
• 224426-58-8 E-2-methyl-1-phenylhept-6-en-1-one dimethylhydrazone 
• 107112-14-1 2-Methyl-2-phenethyl-3-phenyl-2H-azirine 
• 70200-80-5 Trimethyl-2,2,4 diphenyl-3,5 2H-pyrrole 
• 146431-09-6 N,N-dimethylhydrazone de methyl-2 phenyl-1 pentene-4 one 

Relevant academic research and scientific papers

Synthesis of isoquinolines via Rh(III)-catalyzed C-H activation using hydrazone as a new oxidizing directing group

An efficient and mechanistically interesting method for the synthesis of highly substituted isoquinolines by a Rh(III)-catalyzed hydrazone directed ortho C-H bond activation and annulation without an external oxidant is described. This reaction is accomplished via a C-C and C-N bond formation along with N-N bond cleavage.

Regio- and stereoselectivity in the cyclization of enolates derived from 4,5-, 5,6-, and 6,7-epoxy-1-phenyl-1-alkanones. Competition between C- and O- alkylation

The results obtained in the base-catalyzed intramolecular cyclization of enolates derived from some representative 4,5-, 5-6, and 6,7-epoxy ketones and of the corresponding alkenes are discussed. The LHMDS/Sc(OTf)3 protocol on epoxy ketones app

Synthese de methyl-8 dehydro-1,2 pyrrolizidines et de methyl-9 dehydro-1,2 indolizidines

A synthetic route to the title compounds is described.It is based on the intramolecular cyclisation of hydroxy-Δ-3-pyrrolines 9, which are prepared in two steps from 2H-pyrroles 4.The stereoselectivity of the sequence can be controlled by changing the order of these two steps.