3-(Trifluoromethyl)benzoic acid structure 
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        Common Name | 3-(Trifluoromethyl)benzoic acid | ||
|---|---|---|---|---|
| CAS Number | 454-92-2 | Molecular Weight | 190.119 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 237.7±0.0 °C at 760 mmHg | |
| Molecular Formula | C8H5F3O2 | Melting Point | 104-106 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 102.9±27.3 °C | |
| Symbol | 
             
            
            GHS07  | 
        Signal Word | Warning | |
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                        The many roles for fluorine in medicinal chemistry.
                        
                        
                         J. Med. Chem. 51 , 4359-69, (2008) 
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                        Studies on the metabolism of fluorinated xenobiotics in the rat using 19F-NMR and 1H-NMR spectroscopy.
                        
                        
                         J. Pharm. Biomed. Anal. 8(8-12) , 939-44, (1990) 
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                        Bacterial metabolism of side chain fluorinated aromatics: cometabolism of 3-trifluoromethyl(TFM)-benzoate by Pseudomonas putida (arvilla) mt-2 and Rhodococcus rubropertinctus N657.
                        
                        
                         Arch. Microbiol. 149(3) , 188-97, (1988) The TOL plasmid-encoded enzymes of the methylbenzoate pathway in Pseudomonas putida mt-2 cometabolized 3-trifluoromethyl (TFM)-benzoate. Two products, 3-TFM-1,2-dihydroxy-2-hydrobenzoate (3-TFM-DHB) and 2-hydroxy-6-oxo-7,7,7-trifluoro-hepta-2,4-dienoate (7-TF...  | 
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                        Degradation of meta-trifluoromethylbenzoate by sequential microbial and photochemical treatments.
                        
                        
                         FEMS Microbiol. Lett. 110(2) , 213-6, (1993) m- and p-trifluoromethyl (TFM)-benzoates are incompletely degraded by aerobic bacteria that catabolize alkylbenzoates; biodegradation ceases after ring-fission with the accumulation of a trifluoromethyl muconate semialdehyde (2-hydroxy-6-oxo-7,7,7-trifluorohe...  | 
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                        Regioselective dioxygenation of ortho-trifluoromethylbenzoate by Pseudomonas aeruginosa 142: evidence for 1,2-dioxygenation as a mechanism in ortho-halobenzoate dehalogenation.
                        
                        
                         Biochem. Biophys. Res. Commun. 213(3) , 759-67, (1995) Pseudomonas aeruginosa strain 142 oxidizes 2-halobenzoates via a multicomponent oxygenase (V. Romanov and R.P. Hausinger, J. Bacteriol., 1994, 176(11), 3368-3374). The intermediacy of a highly unstable cis-diol in the reaction has been proposed. Direct eviden...  | 
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                        Polymeric drugs with prolonged sustained delivery of specific anti-aggregant agents for platelets: kinetic analysis of the release mechanism.
                        
                        
                         J. Biomater. Sci. Polym. Ed. 15(7) , 917-28, (2004) The in vitro aqueous behaviour of a metacryloyloxyethyl [2-(acetyloxy)-4-(trifluoromethyl)]benzoate (THEMA)/N,N'-dimethylacrylamide (DMA) copolymer with a THEMA molar content of 39% (labeled THDMA39) has been investigated. This composition has been selected t...  | 
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                        Dissociation constants of neutral and charged acids in methyl alcohol. The acid strength resolution. Rived F, et al.
                        
                        
                         Anal. Chim. Acta 374(2) , 309-324, (1998) 
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                        Solubility of fluorinated pharmaceuticals in dense carbon dioxide. Laitinen A, et al.
                        
                        
                         Org. Process Res. Dev. 4(5) , 353-6, (2000) 
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