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| Names | |
|---|---|
| Preferred IUPAC name 4-(4-Methylphenyl)-4-oxobutanoic acid | |
| Other names 3-(4-Methylbenzoyl)propionic acid 3-(p-Toluoyl)propionic acid 4-(4-Methylphenyl)-4-oxobutyric acid | |
| Identifiers | |
3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.118.705 |
| EC Number |
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PubChem CID | |
| UNII | |
CompTox Dashboard (EPA) | |
| |
| |
| Properties | |
| C11H12O3 | |
| Molar mass | 192.214 g·mol−1 |
| Appearance | White powder |
| Melting point | 129 °C (264 °F; 402 K) |
| Insoluble | |
| Hazards [1] | |
| Occupational safety and health (OHS/OSH): | |
Main hazards | Flammable |
| GHS labelling: | |
| | |
| Warning | |
| H315, H319, H335 | |
| P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
4-(4-Methylphenyl)-4-oxobutanoic acid is an organic carboxylic acid. The preparation of it is used for undergraduate teaching of organic chemistry synthesis.
4-(4-Methylphenyl)-4-oxobutanoic acid can be prepared by a Friedel–Crafts reaction between toluene and succinic anhydride catalyzed by a Lewis acid such as aluminium chloride. [2]