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2,3-DIMETHOXYBENZONITRILE

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2,3-DIMETHOXYBENZONITRILE Basic information

Product Name:
2,3-DIMETHOXYBENZONITRILE
Synonyms:
  • LABOTEST-BB LT00159775
  • BENZONITRILE, 2,3-DIMETHOXY-
  • AKOS BBS-00004470
  • AKOS B004317
  • 3-CYANOVERATROLE
  • 3,4-DIMETHOXYBENZONITRILE
  • 4-CYANO-1,2-DIMETHOXYBENZENE
  • 4-CYANOVERATROLE
CAS:
2024-83-1
MF:
C9H9NO2
MW:
163.17
EINECS:
217-969-2
Product Categories:
  • Verapamil/Denopamine
  • Building Blocks
  • C8 to C9
  • Chemical Synthesis
  • Nitrogen Compounds
  • Organic Building Blocks
  • Aromatic Nitriles
  • Phenyls & Phenyl-Het
  • Nitrile
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Phenyls & Phenyl-Het
  • C8 to C9
  • Cyanides/Nitriles
  • Nitrogen Compounds
  • Nitriles
Mol File:
2024-83-1.mol
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2,3-DIMETHOXYBENZONITRILE Chemical Properties

Melting point:
68-70 °C(lit.)
Boiling point:
290.25°C (rough estimate)
Density 
1.2021 (rough estimate)
refractive index 
1.5300 (estimate)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
Soluble in methanol.
form 
powder to crystal
color 
White to Light yellow
BRN 
1451651
CAS DataBase Reference
2024-83-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,T,Xi
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36
RIDADR 
3276
WGK Germany 
3
RTECS 
DI4355000
HazardClass 
6.1
PackingGroup 
III
HS Code 
2926907090

MSDS

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2,3-DIMETHOXYBENZONITRILE Usage And Synthesis

Chemical Properties

white to light yellow crystal powder

Uses

3,4-Dimethoxybenzonitrile is used as an organic chemical synthesis intermediate.

Preparation

Veratraldoxime(88–89 g, 0.45 mol) was combined with acetic anhydride (100 g) in a 300-mL round-bottomed flask equipped with a ground-glass air condenser, and the mixture was cautiously heated. A vigorous reaction took place, at which point the flame (heating by oil bath; the author) was removed. After the reaction had subsided, the solution was gently refluxed for 2 h and then carefully poured, with stirring, into cold water (300 mL). Stirring was continued, and on cooling the nitrile separated as small, almost colorless crystals; these were collected by filtration and dried in air. The veratronitrile thus obtained was quite pure; yield 57–62 g (72–76%); mp 66–67 C°.

1-Cyanoacenaphthene 1403 can be synthesized from its carbaldoxime by dehydration with acetic anhydride in 87% yield. Whereas acetic anhydride usually serves as the solvent as well as the reactant, this procedure is performed in n-octane.

Synthesis Reference(s)

Synthesis, p. 510, 1985 DOI: 10.1055/s-1985-31253

2,3-DIMETHOXYBENZONITRILE Preparation Products And Raw materials

Raw materials

2,3-DIMETHOXYBENZONITRILESupplier

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