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 | |
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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 | |
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). | |
verify (what is ?) | |
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]
Original source: https://en.wikipedia.org/wiki/4-(4-Methylphenyl)-4-oxobutanoic acid.
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