- Apremilast Impurity 59
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- $0.00 / 10mg
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2024-08-28
- CAS:2024-83-1
- Min. Order: 10mg
- Purity: 0.98
- Supply Ability: 10g
- Veratronitrile
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- $12.00 / 25g
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2024-08-07
- CAS:2024-83-1
- Min. Order: 25g
- Purity: 0.98
- Supply Ability: 25kg
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| 2,3-DIMETHOXYBENZONITRILE Basic information |
| 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) | Fp | >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) |
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 |
| 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°.
![2024-83-1 synthesis](https://www.chemicalbook.com/NewsImg/2020-05-12/20205121532275902.jpg)
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 |
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