| Bioactivity | 4-(Phenylcarbonyl)benzoic acid is a photooxidant. Upon light activation, 4-(Phenylcarbonyl)benzoic acid forms an electrophilic aromatic ketone that acts as an oxidant in organic synthesis or biological systems. 4-(Phenylcarbonyl)benzoic acid has been used in the study of amino acid oxidation, as well as the synthesis of photoactivated antibacterial and antiviral compounds123. | ||||||
| CAS | 611-95-0 | ||||||
| Formula | C14H10O3 | ||||||
| Molar Mass | 226.23 | ||||||
| Appearance | 固体 | ||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||
| Storage | Store at room temperature 3 years
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| Reference | [1]. Cohen SG, et al. Letter: Photooxidation of methionine and related compounds. J Am Chem Soc. 1975 Sep 17;97(19):5633-4. [2]. Bobrowski K, et al. 4-Carboxybenzophenone-sensitized photooxidation of sulfur-containing amino acids. Nanosecond laser flash photolysis and pulse radiolysis studies[J]. Journal of the American Chemical Society, 1992, 114(26): 10279-10288. [3]. Xu M, et al. Olfactory perception and behavioral effects of sex pheromone gland components in Helicoverpa armigera and Helicoverpa assulta. Sci Rep. 2016 Mar 15;6:22998. doi: 10.1038/srep22998. Erratum in: Sci Rep. 2016 Apr 29;6:24814. |
4-Benzoylbenzoic acid
CAS: 611-95-0 F: C14H10O3 W: 226.23
4-(Phenylcarbonyl)benzoic acid is a photooxidant. Upon light activation, 4-(Phenylcarbonyl)benzoic acid forms an electro
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