6946-08-3

Usage

General Description

2-amino-2-methyl-1-phenylpropan-1-one, also known as Methamphetamine, is a powerful and highly addictive central nervous system stimulant. It is a synthetic drug that affects the brain and can lead to serious health problems, including addiction. Methamphetamine is commonly abused for its intense euphoria and long-lasting high, making it highly sought after as a recreational drug. The drug is typically ingested orally, injected, snorted, or smoked, and its effects can last for hours. Long-term use of Methamphetamine can lead to severe physical and psychological issues, including heart problems, dental issues, weight loss, and paranoia. Additionally, the manufacturing process for Methamphetamine involves hazardous chemicals and can result in environmental contamination. Due to its highly addictive nature and harmful effects, Methamphetamine is classified as a Schedule II controlled substance in the United States, making it illegal to possess or distribute without a prescription.

Upstream product

• 18262-77-6 isopropyloxy-2 phenyl-2 dimethyl-3,3 aziridine 
• 46365-52-0 α-Amino-isobutyrophenon-dimethylketal 
• 66434-08-0 2-amino-2-methyl-1-phenylpropan-1-one oxime 
• 56062-73-8 iodure de N,N,N-trimethyl hydrazonium de l'isobutyrophenon 
• 721388-02-9 N,N,N-Trimethyl-N'-[2-methyl-1-phenyl-prop-(Z)-ylidene]-hydrazinium 
• 14491-02-2 2,2-dimethyl-3-phenyl-2H-azirine 
• 611-70-1 phenyl isopropyl ketone 
• 121787-97-1 tert-butyldimethyl((2-methyl-1-phenylprop-1-en-1-yl)oxy)silane 
• 36238-46-7 2-Chlorisobutyrophenonoxim 
• 768-49-0 (2-methyl-1-propenyl)-benzene 

Downstream Products

• 58417-75-7 5-hydroxy-4,4-dimethyl-5-phenyl-thiazolidine-2-thione 
• 75416-23-8 amino-2 methyl-2 phenyl-3 pentanol-3 
• 74279-96-2 2-benzoyl-2-(N,N-dichloroamino)propane 
• 75189-02-5 2-Aminoisobutyrophenon-p-nitrophenylhydrazon-hydrochlorid 
• 75189-03-6 2-Aminoisobutyrophenon-2,4-dinitrophenylhydrazon 
• 850232-79-0 2-tert-butyl-ONN-azoxy-2-benzoylpropane 
• 74279-97-3 2-(1,1-Dimethyl-2-oxo-2-phenyl-ethylazo)-2-methyl-1-phenyl-propan-1-one 
• 1260435-37-7 methyl 2-(2-methyl-1-oxo-1-phenylpropan-2-ylamino)-2-oxoacetate 
• 1260435-35-5 N-(2-methyl-1-oxo-1-phenylpropan-2-yl)nicotinamide 
• 1260435-36-6 (S)-benzyl 1-(2-methyl-1-oxo-1-phenylpropan-2-ylamino)1-oxopropan-2-ylcarbamate 
• 1260435-59-3 5-ethoxy-4,4-dimethyl-2,5-diphenyl-4,5-dihydrooxazole 
• 210898-28-5 5,5-dimethyl-3,6-diphenyl-5,6-dihydro-4H-1,2,4-oxadiazin-6-ol 
• 1260435-56-0 2,5,5-trimethyl-3,6-diphenyl-2,5-dihydro-1,2,4-triazine 
• 1260435-54-8 5,5-dimethyl-6-phenyl-3-(pyridin-3-yl)-4,5-dihydro-1,2,4-triazine 

Relevant academic research and scientific papers

Aza-Rubottom Oxidation: Synthetic Access to Primary α-Aminoketones

An aza analogue of the Rubottom oxidation is reported. This facile transformation takes place at ambient temperature and directly converts silyl enol ethers to the corresponding primary α-aminoketones. The use of hexafluoroisopropanol (HFIP) as the solven

RADICAL STABILISATION: SYNTHESIS AND DECOMPOSITION OF A β-KETODIAZENE

The synthesis and decomposition of bis(1,1-dimethyl-2-oxo-2-phenylethyl)diazene (7e) is described.The presence of a carbonyl group adjacent to a radical center greatly enhances the radical stability.

Cyclization of Non-tautomerizing anti-α-Aminohydrazones into N-Aminoimidazolidines

The α-aminoisobutyrophenone phenylhydrazones 3a-h have been prepared and their anti-configuration determined UV spectroscopically.Cyclization of 3 with phosgene yields the hexahydrotetrazine derivatives 5 which react with water to give the 3-anilino-4-hyd

HYDROBORATION D'AZIRIDINES ETHYLENIQUES. SYNTHESE D'AZA-1 BICYCLO ALCANES

Hydroboration of aziridines having a β or γ-double bond 3b, 3c, 4b, 7c and 8 yields after oxydation, the expected hydroxy aziridines 11b, 11c, 12b, 13 and 14, which were cyclized by reaction with PPh3/Br2 to give 1-aza bicycloalkanes 23b, 24b, 25c, 26 and 27.The hydroboration of 2-vinyl aziridines 3a, 4a and 7a give Z-allylic amines 16aZ, 17aZ and 18Z.The use of 9-BBN or 2-vinyl substituated aziridines provides the β-hydroxy aziridines 19, 20 and 21.