2,3-DIMETHOXYBENZONITRILE
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
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)
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
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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
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