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42797-18-2

42797-18-2 Structure

42797-18-2 Structure
IdentificationBack 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
Chemical PropertiesBack Directory
[Melting point ]

225-227℃
[Boiling point ]

539.3±43.0 °C(Predicted)
[density ]

1.232
[vapor pressure ]

0-0Pa at 25℃
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

Solid:particulate/powder
[pka]

3.34±0.36(Predicted)
[color ]

White to Almost white
[LogP]

1.78 at 25℃
[EPA Substance Registry System]

Benzoic acid, 2-([1,1'-biphenyl]-4-ylcarbonyl)- (42797-18-2)
Safety DataBack Directory
[RTECS ]

DG4375000
[TSCA ]

TSCA listed
[HS Code ]

2918.30.9000
[REACH Registrations]

Active
[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 InformationBack Directory
[Synthesis]

Phthalic anhydride

85-44-9

Biphenyl

92-52-4

o-(4-Biphenylylcarbonyl)benzoic acid

42797-18-2

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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