79278-71-0

Usage

Chemical classification

Synthetic cathinone

Psychoactive properties

Stimulant

Mechanism of action

Norepinephrine-dopamine reuptake inhibitor

Appearance

Found in "bath salt" products

Recreational use

Gained popularity due to powerful stimulating effects

Effects

Heightened euphoria, increased alertness, and surge of energy

Risks

Substantial risks of addiction and adverse health effects

Legal status

Classified as a controlled substance in many countries

Regulation

Production, distribution, and sale are heavily regulated

Prevalence

Use has declined in recent years, but remains a concern in illicit drug abuse and law enforcement.

Upstream product

• 39742-60-4 1-(2-phenylethyl)-4-piperidinone 

Downstream Products

• 51448-56-7 4-amino-1-(2-phenylethyl)-piperidine 
• 118142-37-3 N-(1-phenethylpiperidine-4-yl)furan-2-carboxamide 
• 118142-38-4 N-(1-phenethylpiperidine-4-yl)furan-3-carboxamide 
• 974-10-7 N-(1-phenethylpiperidin-4-yl)benzamide 
• 127285-07-8 1-phenethylpiperidin-4-amine hydrochloride 
• 117523-79-2 Furan-3-carboxylic acid benzothiazol-2-yl-(1-phenethyl-piperidin-4-yl)-amide 
• 117523-76-9 Furan-3-carboxylic acid benzooxazol-2-yl-(1-phenethyl-piperidin-4-yl)-amide 
• 117523-78-1 Furan-2-carboxylic acid benzothiazol-2-yl-(1-phenethyl-piperidin-4-yl)-amide 
• 117523-75-8 Furan-2-carboxylic acid benzooxazol-2-yl-(1-phenethyl-piperidin-4-yl)-amide 
• 117523-51-0 N-(4-chloro-pyrimidin-6-yl)-N-[1-(2-phenylethyl)-4-piperidyl]-3-furamide 
• 117523-50-9 Furan-3-carboxylic acid (2-chloro-pyrimidin-4-yl)-(1-phenethyl-piperidin-4-yl)-amide 
• 117523-71-4 Furan-2-carboxylic acid (6-chloro-pyrimidin-4-yl)-(1-phenethyl-piperidin-4-yl)-amide 
• 117523-69-0 N-(2-chloro-pyrimidin-4-yl)-N-[1-(2-phenylethyl)-4-piperidyl]-2-furamide 
• 117523-77-0 N-Benzothiazol-2-yl-2-methoxy-N-(1-phenethyl-piperidin-4-yl)-acetamide 

Relevant academic research and scientific papers

Hyperpolarisation of Mirfentanil by SABRE in the Presence of Heroin

Mirfentanil, a fentanyl derivative that is a μ-opioid partial agonist, is hyperpolarised via Signal Amplification By Reversible Exchange (SABRE), a para-hydrogen-based technique. [Ir(IMes)(COD)Cl] (IMes=1,3-bis(2,4,6-trimethylphenyl)imidazole-2-ylidene, C

SUBSTITUTED 1-ARYLETHYL-4-ACYLAMINOPIPERIDINE DERIVATIVES AS OPIOID/ALPHA-ADRENORECEPTOR MODULATORS AND METHOD OF THEIR PREPARATION

The invention provides compounds that bind with high affinities to the μ-, δ- and κ- opioid receptors and α2 - adrenoreceptor. In addition to providing these compounds with novel pharmacological binding properties, the invention also describes detailed novel methods for the preparation of representative compounds and a scheme for the synthesis of related compounds that bind to the opioid receptors and/or α2 - adrenoreceptor.