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(alphaR)-alpha-[[[2-(4-Aminophenyl)ethyl]amino]methyl]benzenemethanol hydrochloride

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(alphaR)-alpha-[[[2-(4-Aminophenyl)ethyl]amino]methyl]benzenemethanol hydrochloride Basic information

Product Name:
(alphaR)-alpha-[[[2-(4-Aminophenyl)ethyl]amino]methyl]benzenemethanol hydrochloride
Synonyms:
  • (alphaR)-alpha-[[[2-(4-Aminophenyl)ethyl]amino]methyl]benzenemethanol hydrochloride
  • (R)-alpha-[[[2-(4-AMinophenyl)ethyl]aMino]Methyl]
  • (R)-2-[2-(4-Amino-phenyl)-ethylamino]-1-phenyl-ethanol HCl
  • (R)-[[[2-(4-aMinophenyl)ethyl]aMino]Methyl]- BenzeneMethanol HCl
  • (R)--[[[2-(4-aminophenyl)ethyl]amino]methyl]-Benzenemethanol
  • Mirabegron INT 3
  • (R) -2 - [[2- (4- aminophenyl) ethyl] amino] -1-phenylethanol hydrochloride
  • (R)-2-((4-AMinophenethyl)aMino)-1-phenylethanol hydrochloride
CAS:
521284-22-0
MF:
C16H21ClN2O
MW:
292.81
EINECS:
700-425-8
Product Categories:
  • 521284-22-0
Mol File:
521284-22-0.mol
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(alphaR)-alpha-[[[2-(4-Aminophenyl)ethyl]amino]methyl]benzenemethanol hydrochloride Chemical Properties

Density 
1145 at 20℃
vapor pressure 
0.015Pa at 25℃
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Powder
Stability:
Hygroscopic
LogP
-1.35 at 20℃ and pH5.79
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(alphaR)-alpha-[[[2-(4-Aminophenyl)ethyl]amino]methyl]benzenemethanol hydrochloride Usage And Synthesis

Uses

(alphaR)-alpha-[[[2-(4-Aminophenyl)ethyl]amino]methyl]benzenemethanol hydrochloride can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development processes and chemical production processes.

Synthesis


A mixture of (100 g) (R)-2-[2?ˉ -(4-nitrophenyl)ethyl]amino] -1 -phenylethanol monohydroch bride (prepared according to example Ib), methanol (2000 mL) and Raney Nickel (20 g, wet) was stirred under hydrogen pressure (60 psi) for 6 hrs. The reaction solution was filtered, and the filtrate was concentrated in vacuo. The residue was mixed with isopropanol (300 mL) and reaction mixture was heated to 78??C (?à2). The mixture was added to toluene (900 mL). The reaction mixture was gradually cooled to 28??C (?à2) and stirred at this temperature for 3 hrs. The solid obtained was filtered, washed with toluene and dried under vacuo at 48??C (?à2) to obtain (R)-2-[[2-(4-aminophenyl)ethyl]-amino]- I -phenylethanol monohydrochioride.Yield: 78.1 g (86.1%); Purity by HPLC: 99.14 %.

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