72739-14-1

Basic information

• Product Name: S(-)-CATHINONE HYDROCHLORIDE
• Synonyms: S(-)-2-AMINO-1-PHENYL-1-PROPANONE HYDROCHLORIDE;S(-)-CATHINONE HYDROCHLORIDE;Methanol（Test S(-)-Cathinone HCl, 1.0 mg/mL as free base）;S(-)-Cathinone HCl;S(-)-Cathinone hydrochloride solution;()-(S)-Cathinone (hydrochloride) (exempt preparation);(2S)-2-amino-1-phenylpropan-1-one:hydrochloride
• CAS NO: 72739-14-1
• Molecular Formula: C₉H₁₁NO*ClH
• Molecular Weight: 185.65
• EINECS: 200-659-6
• Mol File: 72739-14-1.mol
• Article Data: 6

Chemical Properties

• Flash Point: 9℃
• Appearance: /
• Storage Temp.: ?20°C
• CAS DataBase Reference: S(-)-CATHINONE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: S(-)-CATHINONE HYDROCHLORIDE(72739-14-1)
• EPA Substance Registry System: S(-)-CATHINONE HYDROCHLORIDE(72739-14-1)

Safety Data

• Hazard Codes: F,T
• Statements: 11-23/24/25-39/23/24/25
• Safety Statements: 7-16-36/37-45
• RIDADR: UN1230 - class 3 - PG 2 - Methanol, solution
• WGK Germany: 1
• Hazardous Substances Data: 72739-14-1(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

Uses

Psychoactive alkaloid found in the leaves of the khat plant, Catha edulis Forsk., Celastraceae. Controlled substance (stimulant).

General Description

This Certified Spiking Solution? is suitable for GC/MS or LC/MS testing applications involving cathinone in clinical toxicology, forensic analysis or urine drug testing. Cathinone, or benzoylethanamine, is a major active constituent of the recreational drug “Khat”. This stimulant has also been found in illicit bath salts.

Upstream product

• 81626-23-5 (-)-N-formyl-α-aminopropiophenone 
• 53630-90-3 (-)-norephedrine formate 
• 77387-33-8 (1R,2S)-(-)-N-formylnorephedrine 
• 113322-99-9 tert-butyl ((1R,2S)-1-hydroxy-1-phenylpropan-2-yl)carbamate 
• 2114-00-3 2-bromo-1-phenyl-1-propanone 
• 35947-99-0 2-azido-1-phenyl-1-propanone 
• 225098-33-9 tert-butyl ((2S)-1-hydroxy-1-phenylpropan-2-yl)carbamate 
• 108-86-1 bromobenzene 
• 159434-78-3 (-)-(1R,2S)-2-Azido-1-(tert-butyldimethylsiloxy)-1-phenylpropane 
• 79821-73-1 (S)-N-(1-Methyl-2-oxo-2-phenylethyl)carbamidsaeure-(tert-butyl)ester 

Downstream Products

• 79821-73-1 (S)-N-(1-Methyl-2-oxo-2-phenylethyl)carbamidsaeure-(tert-butyl)ester 
• 71031-15-7 cathinone 
• 80096-54-4 (R)-β‐ketoamphetamine 

Relevant articles and documents

A practical synthesis of α-amino ketones via aryllithium addition to N-Boc-α-amino acids

The reaction of N-Boc-α-amino acids with aryllithium reagents followed by removal of the nitrogen protecting group provides enantiomerically pure α-amino aryl ketones as their corresponding HCl salts. This practical two-step sequence gives rapid access to a pharmaceutically interesting class of compounds from commercially available starting materials.

Rearrangement of N-tert-butanesulfinyl α-halo imines with alkoxides to N-tert-butanesulfinyl 2-amino acetals as precursors of N-protected and N-unprotected α-amino carbonyl compounds

Reaction of N-tert-butanesulfinyl α-halo imines with alkoxides afforded new N-tert-butanesulfinyl 2-amino acetals in good to excellent yield. These N-tert-butanesulfinyl 2-amino acetals are convenient precursors for the TMSOTf-promoted synthesis of the co

Enantioselective synthesis of both enantiomers of cathinone via the microbiological reduction of 2-azido-1-phenyl-1-propanone

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