Identification | Back Directory | [Name]
o-(4-Biphenylylcarbonyl)benzoic acid | [CAS]
42797-18-2 | [Synonyms]
o-(4-Biphenylylcarbonyl) 2-(4-Phenylbenzoyl)benzoic acid o-(4-Biphenylylcarbonyl)benzoic acid 2-(4-Biphenylylcarbonyl)benzoic acid 2-(biphenyl-4-ylcarbonyl)benzoic acid 2-(4-Biphenylylcarbonyl)benzoic Acid > 2-[(4-phenylphenyl)carbonyl]benzoic acid o-(1,1'-Biphenyl-4-ylcarbonyl)benzoic acid Benzoic acid, 2-([1,1'-biphenyl]-4-ylcarbonyl)- | [EINECS(EC#)]
200-258-5 | [Molecular Formula]
C20H14O3 | [MDL Number]
MFCD00392368 | [MOL File]
42797-18-2.mol | [Molecular Weight]
302.33 |
Safety Data | Back Directory | [RTECS ]
DG4375000 | [HS Code ]
2918.30.9000 | [Toxicity]
mouse,LDLo,intraperitoneal,500mg/kg (500mg/kg),"Summary Tables of Biological Tests," National Research Council Chemical-Biological Coordination Center. Vol. 4, Pg. 107, 1952. |
Hazard Information | Back Directory | [Synthesis]
The general procedure for the synthesis of O-(4-biphenylyl)benzoic acid from phthalic anhydride and biphenyl was as follows: 154.0 g (1.0 mol) of biphenyl and 148.0 g (1.0 mol) of phthalic anhydride were homogeneously dispersed in 800 ml of dichloromethane. Subsequently, 226.0 g (2 moles) of aluminum trichloride was added in batches under cooling conditions in a water bath, and the reaction temperature was controlled not to exceed 20 °C. After addition, the reaction mixture was stirred at room temperature overnight and observed to gradually change to light blue color. Next, the reaction mixture was slowly poured into a mixture consisting of 3.0 liters of water, 500 grams of crushed ice, and 400 grams of sulfuric acid under continuous stirring. During this process, the blue color gradually faded while a white precipitate was produced. The precipitate was separated by filtration and washed with 4 x 300 ml of water and finally dried. The mass of the product obtained was 291.0 g and the yield was 96% of the theoretical value. The product was characterized by the following data: GC purity 98%; melting point 232-233°C; GC purity 99%; mass spectra (m/z): 374 (M+ -1 + 73 (trimethylsilane)), 359 (100%), 285, 228, 181, 152, 73; UV spectrum: λmax = 286 nm (ethanol). | [References]
[1] Patent: WO2015/164205, 2015, A1. Location in patent: Paragraph 0099; 0062 [2] Bulletin de la Societe Chimique de France, 1980, vol. 2, # 7-8, p. 334 - 344 [3] Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1983, vol. 32, # 4, p. 853 - 855 [4] Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1983, # 4, p. 941 - 943 [5] Chemische Berichte, 1911, vol. 44, p. 1078 |
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