AKOS BBS-00004326
2',5'-Dimethoxyacetophenone
CAS: 1201-38-3
Molecular Formula: C10H12O3
AKOS BBS-00004326 - Names and Identifiers
| Name | 2',5'-Dimethoxyacetophenone |
| Synonyms | AKOS BBS-00004326 2',5'-Dimethoxyaceto 2,5-Dimethoxyacetophenone 2[,5[-Dimethoxyacetophenone 2,5-Dimethoxy acetonphenone 2',5'-Dimethoxyacetophenone Acetophenone, 2',5'-dimethoxy- 1-(2,5-dimethoxyphenyl)-ethanon 1-(2,4-dimethoxyphenyl)ethanone 1-(2,5-dimethoxyphenyl)ethanone 1-(2,5-dimethoxyphenyl)-ethanone Methyl 2,5-dimethoxyphenyl ketone Ethanone,1-(2,5-dimethoxyphenyl)- |
| CAS | 1201-38-3 |
| EINECS | 214-858-0 |
| InChI | InChI=1/C10H12O3/c1-7(11)9-6-8(12-2)4-5-10(9)13-3/h4-6H,1-3H3 |
| InChIKey | FAXUIYJKGGUCBO-UHFFFAOYSA-N |
AKOS BBS-00004326 - Physico-chemical Properties
| Molecular Formula | C10H12O3 |
| Molar Mass | 180.2 |
| Density | 1.139g/mLat 25°C(lit.) |
| Melting Point | 18-20°C(lit.) |
| Boling Point | 155-158°C11mm Hg(lit.) |
| Flash Point | >230°F |
| Solubility | Chloroform, Methanol (Slightly) |
| Vapor Presure | 0.00164mmHg at 25°C |
| Appearance | Crystalline powder |
| Color | Clear yellow to green-yellow |
| BRN | 2047423 |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | n20/D 1.5441(lit.) |
| MDL | MFCD00008728 |
AKOS BBS-00004326 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| TSCA | Yes |
| HS Code | 29145090 |
| Hazard Class | IRRITANT |
AKOS BBS-00004326 - Reference Information
| NIST chemical information | Information provided by: webbook.nist.gov (external link) |
| EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
| introduction | 2,5-dimethoxyacetophenone is the representative substance of such compounds. it is a transparent yellow liquid with a density of 1.139 g/ml at 25 c (lit.) and a boiling point of 155-158 c 11mm Hg(lit.). |
| preparation | weigh 5g of 2,5-dimethoxybenzene sample in a 100 ml three-mouth flask, dissolve with 10 ml of carbon tetrachloride, add 5. 5g of anhydrous aluminum trichloride, and stir with magnets; Under the condition of ice bath , 3.5 ml of acetyl chloride (diluted with 10 ml of carbon tetrachloride) is added dropwise at a rate of 30 drops per minute. The resulting hydrogen chloride is introduced into the sodium hydroxide absorption cell. The reaction time is 1. 5 hours. Then at room temperature, react for another 5 hours. The reaction mixture is washed with hydrochloric acid ice water mixture, ethyl acetate is extracted twice, the organic phase of the extract is combined, magnesium sulfate is dried, and left overnight . Rotary evaporation removes ethyl acetate. Column separation, ethyl acetate: petroleum ether = 1:5 as eluent. The target compound 2, 5-dimethoxyacetophenone was obtained. |
Last Update：2024-04-09 21:04:16
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