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3,4-dimethoxy-alpha-methylphenethylamine

  • Name: 3,4-dimethoxy-alpha-methylphenethylamine
  • CAS: 120-26-3
  • Purity: 99%
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  • Description

    Manufacturer Supply Best Quality 3,4-dimethoxy-alpha-methylphenethylamine 120-26-3 with Efficient Transportation

    • Molecular Formula: C11H17 N O2
    • Molecular Weight: 195.261
    • Melting Point: 39-40 °C 
    • Boiling Point: 289°Cat760mmHg 
    • PKA: 9.78±0.10(Predicted) 
    • Flash Point: 139.8°C 
    • PSA： 44.48000 
    • Density: 1.023g/cm3 
    • LogP: 2.29380 

    120-26-3 Relevant articles

    Transaminase-mediated synthesis of enantiopure drug-like 1-(3′,4′-disubstituted phenyl)propan-2-amines

    Lakó, ágnes,Mendon?a, Ricardo,Molnár, Zsófia,Poppe, László

    , p. 40894 - 40903 (2020/11/23)

    Transaminases (TAs) offer an environment...

    Stereoselective Synthesis of 1-Arylpropan-2-amines from Allylbenzenes through a Wacker-Tsuji Oxidation-Biotransamination Sequential Process

    González-Martínez, Daniel,Gotor, Vicente,Gotor-Fernández, Vicente

    , p. 2582 - 2593 (2019/05/15)

    Herein, a sequential and selective chemo...

    Novel dihydroquinolizinones for the treatment and prophylaxis of hepatitis B virus infection

    -

    Paragraph 100; 1007, (2015/08/04)

    The invention provides novel compounds h...

    NOVEL DIHYDROQUINOLIZINONES FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION

    -

    Page/Page column 116; 117, (2015/09/23)

    The invention provides novel compounds h...

    120-26-3 Process route

    1-(3,4-dimethoxyphenyl)-2-nitropropene
    122-47-4

    1-(3,4-dimethoxyphenyl)-2-nitropropene

    2-(3,4-dimethoxyphenyl)-1-methylethylamine
    120-26-3

    2-(3,4-dimethoxyphenyl)-1-methylethylamine

    Conditions
    Conditions Yield
    1-(3,4-dimethoxyphenyl)-2-nitropropene; With lithium aluminium tetrahydride; In tetrahydrofuran; for 1h; Heating / reflux;
    With hydrogenchloride; In tetrahydrofuran; water; ethyl acetate;
    With ammonia; tartaric acid; more than 3 stages;
    		87%
    With ethanol; sulfuric acid; acetic acid; Electrolysis.an einer Quecksilber-Kathode;
    With lithium aluminium tetrahydride;
    With lithium aluminium tetrahydride; In tetrahydrofuran;
    With lithium aluminium tetrahydride; In tetrahydrofuran; for 14h; Yield given; Heating;
    With lithium aluminium tetrahydride; In tetrahydrofuran; for 3h; Heating;
    		9.4 g
    With lithium aluminium tetrahydride; diethyl ether;
    With lithium aluminium tetrahydride; In tetrahydrofuran; at 20 ℃; for 3h; Reflux;
    With lithium aluminium tetrahydride; In tetrahydrofuran; at 20 ℃; Reflux;
    N-benzyl-α-methyl-3,4-dimethoxyphenethylamine
    58379-94-5

    N-benzyl-α-methyl-3,4-dimethoxyphenethylamine

    2-(3,4-dimethoxyphenyl)-1-methylethylamine
    120-26-3

    2-(3,4-dimethoxyphenyl)-1-methylethylamine

    Conditions
    Conditions Yield
    With hydrogen; palladium on activated charcoal; In methanol; at 40 ℃; for 24h;
    		65%

    120-26-3 Upstream products

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      122-47-4

      1-(3,4-dimethoxyphenyl)-2-nitropropene

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      1,2-dimethoxy-4-(2-propenyl)benzene

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      3-(3,4-dimethoxy-phenyl)-2-methyl-propionic acid amide

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      3,4-dimethoxyphenylacetone

    120-26-3 Downstream products

    • 3979-57-5
      3979-57-5

      (3,4-dimethoxy-phenyl)-acetic acid-[2-(3,4-dimethoxy-phenyl)-1-methyl-ethylamide]

    • 5884-29-7
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      6,7-dimethoxy-3-methyl-3,4-dihydro-isoquinoline; hydrochloride

    • 103330-49-0
      103330-49-0

      N ,N '-bis-[2-(3,4-dimethoxy-phenyl)-1-methyl-ethyl]-adipamide

    • 33236-61-2
      33236-61-2

      1-(3,4-dimethoxyphenyl)-N-methylpropan-2-amine

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