(3,4-Dimethoxyphenyl)acetonitrile

(3,4-Dimethoxyphenyl)acetonitrile
  • CAS No.:93-17-4
Other grades of this product :
(3,4-Dimethoxyphenyl)acetonitrile Basic information
Product Name:(3,4-Dimethoxyphenyl)acetonitrile
Synonyms:3,4-Dimethoxylphenylacetonitrile;(3,4-Dimethoxyphenyl)acetonitrile, 3,4-Dimethoxybenzylcyanide, Homoveratronitrile;(3,4-Dimethoxyphenyl)acetonitrile, 3,4-Dimethoxybenzylcyanide;3,4-dimethoxy-benzeneacetonitril;3,4-dimethoxybenzeneacetonitrile;3,4-dimethoxybenzyl;3,4-dimethoxyphenyl-acetonitril;Acetonitrile, (3,4-dimethoxyphenyl)-
CAS:93-17-4
MF:C10H11NO2
MW:177.2
EINECS:202-225-1
Product Categories:Aromatics, Impurities, Pharmaceuticals, Intermediates & Fine Chemicals;Catechol Derivatives;Aromatic Nitriles;Aromatics;Impurities;Intermediates & Fine Chemicals;Nitriles;Pharmaceuticals
Mol File:93-17-4.mol
(3,4-Dimethoxyphenyl)acetonitrile Chemical Properties
Melting point 54-57 °C(lit.)
Boiling point 171-178 °C10 mm Hg(lit.)
density 1.1607 (rough estimate)
refractive index 1.5168 (estimate)
Fp >230 °F
storage temp. Sealed in dry,Room Temperature
solubility methanol: 0.1 g/mL, clear
form Crystals or Crystalline Needles
color yellow
Water Solubility insoluble
BRN 1956100
Exposure limitsNIOSH: IDLH 25 mg/m3
InChIKeyASLSUMISAQDOOB-UHFFFAOYSA-N
LogP0.915
CAS DataBase Reference93-17-4(CAS DataBase Reference)
NIST Chemistry ReferenceBenzeneacetonitrile, 3,4-dimethoxy-(93-17-4)
Safety Information
Hazard Codes Xn,T
Risk Statements 22-23/24/25-36/37/38-20/21/22
Safety Statements 36/37-45-22-36-26
RIDADR 3276
WGK Germany 3
RTECS AL9325000
HazardClass IRRITANT
HS Code 29269090
MSDS Information
ProviderLanguage
Homoveratronitrile English
SigmaAldrich English
ALFA English
(3,4-Dimethoxyphenyl)acetonitrile Usage And Synthesis
Chemical Propertieswhite to almost white crystals or cryst. needles
UsesAn Impurity of Verapamil (V125000). An intermediate in the preparation of the muscle relaxant Papverine (P190500).
Uses(3,4-Dimethoxyphenyl)acetonitrile has been used in the synthesis of (Z)-3-(benzo[b]thiophen-2-yl)-2-(3,4-dimethoxyphenyl)acrylonitrile. It has also been used in the preparation of modified diterpene (±) nimbidiol which relies on a sulfenium ion promoted polyene cyclization.
Synthesis Reference(s)Journal of the American Chemical Society, 57, p. 1126, 1935 DOI: 10.1021/ja01309a053Tetrahedron Letters, 24, p. 4533, 1983 DOI: 10.1016/S0040-4039(00)85947-X
Purification MethodsIts solubility is 10% in MeOH, and it has been recrystallised from EtOH or MeOH. Purify it also by distillation followed by recrystallisation. [Price & Rogers Org Synth Coll Vol III 174 1955, Niederl & Ziering J Am Chem Soc 64 885 1952, Julian & Sturgis J Am Chem Soc 57 1126 1935, Beilstein 10 I 198.]

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