From Handwiki
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| Names | |
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| 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)
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PubChem CID
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| Properties | |
| C11H12O3 | |
| Molar mass | 192.214 g·mol−1 |
| Appearance | White powder |
| Melting point | 129 °C (264 °F; 402 K) |
| Insoluble | |
| Hazards[1] | |
| Main hazards | Flammable |
| GHS pictograms |
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| GHS Signal word | Warning |
| H315, H319, H335 | |
| P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P332+313, P337+313, P362, P403+233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
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]
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Categories: [Carboxylic acids] [Phenyl compounds] [Aromatic ketones]