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Detail of > 20850-49-1

  • CAS Number:
  • 20850-49-1
  • Name:
  • 3-Methyl-2-(3,4-dimethoxyphenyl)butyronitrile

  • Formula:
  • C13H17NO2
  • Molecular Structure:
  • Synonyms:
  • Butyronitrile,2-(3,4-dimethoxyphenyl)-3-methyl- (8CI);2-(3,4-Dimethoxyphenyl)-3-methylbutanenitrile;3,4-Dimethoxy-a-isopropylbenzeneacetonitrile;Isopropyl(3,4-dimethoxyphenyl)acetonitrile;a-Isopropylhomoveratronitrile;a-Isopropylveratryl cyanide;2-(3,4-Dimethoxyphenyl)-2-isopropylacetonitrile;2-(3,4-Dimethoxyphenyl)-3-methylbutanenitrile;2-(3,4-Dimethoxyphenyl)-3-methylbutyronitrile;3,4-Dimethoxy-a-(1-methylethyl)benzeneacetonitrile;Benzeneacetonitrile, 3,4-dimethoxy-α-(1-methylethyl)-;
  • Molecular Weight:
  • 219.28
  • EINECS:
  • 244-082-8
  • Density:
  • 1.023 g/cm3
  • Melting Point:
  • 46-49 °C
  • Boiling Point:
  • 327.3 °C at 760 mmHg
  • Flash Point:
  • 114.5 °C
  • Appearance:
  • Pale yellow solid
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20850-49-1 3-Methyl-2-(3,4-dimethoxyphenyl)butyronitrile

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20850-49-1 3-Methyl-2-(3,4-dimethoxyphenyl)butyronitrile

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20850-49-1 3-Methyl-2-(3,4-dimethoxyphenyl)butyronitrile

3-Methyl-2-(3,4-dimethoxyphenyl)butyronitrile
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20850-49-1 3-Methyl-2-(3,4-dimethoxyphenyl)butyronitrile

3,4-dimethoxy-(3-methylethyl)phenyl acetonitrile
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20850-49-1 3-Methyl-2-(3,4-dimethoxyphenyl)butyronitrile

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20850-49-1 3-Methyl-2-(3,4-dimethoxyphenyl)butyronitrile

2-(3,4-Dimethoxyphenyl)-3-methylbutyronitrile
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20850-49-1 3-Methyl-2-(3,4-dimethoxyphenyl)butyronitrile

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20850-49-1 3-Methyl-2-(3,4-dimethoxyphenyl)butyronitrile

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    Reference

    Basic substituted phenylacetonitriles
    Basic substituted phenylacetonitriles. Dengel, Ferdinand (Knoll A.-G. Chemische Fabriken, Ger.). Ger. Offen. DE 2631222 19 Jan 1978, 13 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C07C121-66. APPLICATION: DE 76-2631222 12 Jul 1976. DOCUMENT TYPE: Patent CA Section: 25 (Noncondensed Aromatic Compounds) Nine title compds. I (R, R2, R3, R4, R5 = H, halo, alkoxy, R1 = halo, alkoxy, R6 = alkyl) and (or) their HCl and bioxalate salts were prepd. Thus, 3,4-(MeO)2C6H3CH(CHMe2)CN was condensed with ClCH2CH2CH(OEt)2 in refluxing PhMe with addn. of NaNH2 over 3 h to give 84.3% 3,4-(MeO)2C6H3C(CHMe2)(CN)(CH2)2CH(OEt)2, which was ~ quant. hydrolyzed with aq. (CO2H)2 and the resulting aldehyde condensed with 3,4-(MeO2C6H3CH2CH2NH2 in EtOH during hydrogenation over Pd/C to give 92% II, characterized as the HCl salt. 20850-49-1 is the cas registry number. This chemical is also mentioned in this article. .

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