56490-93-8

Basic information

• Product Name: Phenethylamine, alpha,alpha-dimethyl-p-methoxy-, hydrochloride
• Synonyms: Phenethylamine, alpha,alpha-dimethyl-p-methoxy-, hydrochloride;1,1-dimethyl-2-(4-methoxyphenyl)ethylamine hydrochloride;1-(4-methoxyphenyl)-2-methylpropan-2-amine hydrochloride
• CAS NO: 56490-93-8
• Molecular Formula: C₁₁H₁₇NO*ClH
• Molecular Weight: 0
• Mol File: 56490-93-8.mol
• Article Data: 5

Chemical Properties

• Melting Point: 169 °C(Solv: ethanol (64-17-5); ethyl ether (60-29-7))
• Boiling Point: 269.4°Cat760mmHg
• Flash Point: 110.5°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 0.00725mmHg at 25°C
• CAS DataBase Reference: Phenethylamine, alpha,alpha-dimethyl-p-methoxy-, hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: Phenethylamine, alpha,alpha-dimethyl-p-methoxy-, hydrochloride(56490-93-8)
• EPA Substance Registry System: Phenethylamine, alpha,alpha-dimethyl-p-methoxy-, hydrochloride(56490-93-8)

Safety Data

• Hazardous Substances Data: 56490-93-8(Hazardous Substances Data)

Usage

General Description

Phenethylamine, alpha,alpha-dimethyl-p-methoxy-, hydrochloride is a chemical compound that is commonly used as a research chemical and is also found in some prescription medications. It is a derivative of phenethylamine, which is a naturally occurring compound found in the human brain and in certain foods. This particular compound, when used in research, has been shown to have stimulant effects on the central nervous system and is believed to have potential therapeutic applications in the treatment of certain psychiatric disorders. However, due to its stimulant properties and potential for misuse, it is strictly regulated and only available for research and prescription use.

InChI:InChI=1/C11H17NO.ClH/c1-11(2,12)8-9-4-6-10(13-3)7-5-9;/h4-7H,8,12H2,1-3H3;1H

Upstream product

• 110-71-4 1,2-dimethoxyethane 
• 76072-36-1 1-(4-methoxyphenyl)-1-chloro-2-methyl-2-nitropropane 
• 56490-94-9 1-(2-amino-2-methylpropyl)-4-methoxybenzene 
• 16066-97-0 1-nitro-1,1-dimethyl-2-(4-hydroxyphenyl]ethane 
• 824-94-2 p-methoxybenzyl chloride 
• 29206-06-2 2,2-dimethyl-3-(4-methoxyphenyl)propionic acid 
• 1035155-37-3 ethyl 2,2-dimethyl-3-(4-methoxyphenyl)propanoate 
• 85628-47-3 4-Methoxy-(2-methyl-2-nitropropyl)benzol 
• 100-14-1 4-nitrobenzyl chloride 
• 5440-67-5 2-(4-nitrobenzyl)-2-nitropropane 
• 97847-81-9 C₂₃H₂₆NO₂P 
• 79886-12-7 1-(p-aminophenyl)-2-methyl-2-propylamine dihydrochloride 

Downstream Products

• 926319-48-4 6-(phenylmethoxy)-8-[(1R)-1-hydroxy-2-[[2-(4-methoxyphenyl)-1,1-dimethylethyl]amino]ethyl]-2H-1,4-benzoxazin-3(4H)-one hydrochloride 

Relevant articles and documents

IMPROVED PROCESS FOR THE MANUFACTURE OF R-6-HYDROXY-8-[1-HYDROXY-2-[2-(4-METHOXYPHENYL)-1,1-DIMETHYLETHYLAMINOETHYL]-2H-1,4-BENZOXAZIN-3(4H)-ONE HYDROCHLORIDE

The present invention provides an improved process for the manufacture (R)-6- hydroxy-8-[1-hydroxy-2-[2-(4-methoxyphenyl)-1,1-dimethyl-ethylamino-ethyl]-2H-1,4- benzoxazin-3(4H)-one, in high purity and high yield, through the use of 1,1-dimethyl-2- (4-met

1-DIPHENYLPHOSPHINYL-2,2-DIMETHYLAZIRIDINE - A NEW PRECURSOR OF α,α-DIMETHYLARYLALKYLAMINES

The new synthesis of α,α-dimethylarylalkylamines from 1-diphenylphosphinyl-2,2-dimethylaziridine is described.

Novel benzylalcohol derivative and process for preparing the same

A benzylalcohol derivative of the formula: STR1 wherein R is hydroxy, benzyloxy, alkoxy of one to 4 carbon atoms or halogen, and Ring A is monomethoxyphenyl, dimethoxyphenyl, trimethoxyphenyl or 3,4-methylenedioxyphenyl is prepared by reducing a compound of the formula: STR2 wherein R' is benzyloxy, alkoxy of one to 4 carbon atoms or halogen, and Ring A is the same as defined above, and when R' is benzyloxy, if required, further subjecting the product to catalytic hydrogenation. The compounds (I) and pharmaceutically acceptable acid addition salts thereof are used as anti-diabetic agents.