20388-87-8

Basic information

• Product Name: beta-methyl-phenethylaminhydrochloride
• Synonyms: beta-methyl-phenethylaminhydrochloride;beta-Methylphenethylamine hydrochloride;Phenethylamine, beta-methyl-, hydrochloride;2-Phenyl-1-propanamine hydrochloride;2-Phenyl-1-propanamine monohydrochloride;2-Phenylpropylamine hydrochloride;Beta-MethylphenylethylaMine HCl;β-MethylphenethylaMine Hydrochloride
• CAS NO: 20388-87-8
• Molecular Formula: C₉H₁₃N*ClH
• Molecular Weight: 171.66716
• EINECS: 202-303-5
• Mol File: 20388-87-8.mol
• Article Data: 8

Chemical Properties

• Melting Point: 143-144℃
• Boiling Point: 210 °C at 760 mmHg
• Flash Point: 84.6 °C
• Appearance: Cream to pale yellow/Powder
• Vapor Pressure: 0.197mmHg at 25°C
• Sensitive: Hygroscopic
• CAS DataBase Reference: beta-methyl-phenethylaminhydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: beta-methyl-phenethylaminhydrochloride(20388-87-8)
• EPA Substance Registry System: beta-methyl-phenethylaminhydrochloride(20388-87-8)

Safety Data

• Hazardous Substances Data: 20388-87-8(Hazardous Substances Data)

Usage

Description

BMPEA is a phenethylamine compound and positional isomer of amphetamine that has been found in nutritional supplements and classified as a novel doping substance. It acts as an agonist of the human trace amine-associated receptor 1 (EC50s = 325 and 104 nM for R(+) and S(-) isomers, respectively). This product is intended for forensic and research purposes.

Uses

2-phenyl-1-propylamine hydrochloride is an amine organic compound, which can be used as pharmaceutical intermediates.

InChI:InChI=1/C9H13N.ClH/c1-8(7-10)9-5-3-2-4-6-9;/h2-6,8H,7,10H2,1H3;1H

Upstream product

• 582-22-9 2-phenylpropylamine 
• 31731-86-9 2-phenylpropylmagnesium bromide 
• 1634-04-4 tert-butyl methyl ether 
• 1823-91-2 1-phenylethyl cyanide 

Downstream Products

• 1016057-29-6 N-(2-phenylpropyl)-4-(trifluoromethyl)benzamide 
• 582-22-9 2-phenylpropylamine 

Relevant articles and documents

Two-dimensional perovskite chiral ferromagnets

Magnetic molecular materials with a chiral configuration are attractive candidates for sensing, information storage, and spintronics. Herein, we report the first example of two-dimensional hybrid perovskite chiral ferromagnets, (R-MPEA)2CuCl4 and (S-MPEA)2CuCl4. These two compounds exhibit strong oppositely signed circular dichroism signals and clear ferromagnetic behaviors. Magnetic measurements revealed high saturation magnetization up to 12.5 emu g-1. The coexistence of strong chirality and ferromagnetism enabled successful study on their magneto-chiral dichroism spectra. These findings demonstrate a new materials platform for future magneto-optical and spintronic applications, providing insights to the structure-property correlation of chiral ferromagnetic perovskite.

AMPA RECEPTOR POTENTIATORS

The present invention relates to a compound of Formula (I) or a pharmaceutically acceptable salt thereof which is useful for the treatment of conditions associated with glutamate hypofunction, such as psychiatric and neurological disorders.

Process for preparing biphenyl compounds

The present invention relates to a process for the preparation of a biphenyl compound comprising combining a phenyl boronic acid derivative with an halobenzene derivative in the presence of a suitable additive in a suitable organic solvent with a suitable catalyst and a suitable base.