ChemicalBook--->CAS DataBase List--->52938-97-3

52938-97-3

52938-97-3 Structure

52938-97-3 Structure
IdentificationMore
[Name]

5-PHENYL-2-FUROIC ACID
[CAS]

52938-97-3
[Synonyms]

AKOS B025035
AKOS BAR-0049
ASISCHEM V38284
IFLAB-BB F0850-6681
TIMTEC-BB SBB009726
RARECHEM AL BE 0884
ART-CHEM-BB B025035
LABOTEST-BB LT00569128
5-PHENYL-2-FUROIC ACID
5-Phenyl-2-furoic acid 97%
5-PHENYL-2-FURANCARBOXYLIC ACID
5-Phenylfurane-2-carboxylic acid
5-PHENYL-FURAN-2-CARBOXYLIC ACID
5-Phenyl-2-furancarboxylicAcid>
2-Furancarboxylic acid, 5-phenyl-
[Molecular Formula]

C11H8O3
[MDL Number]

MFCD00456304
[Molecular Weight]

188.18
[MOL File]

52938-97-3.mol
Chemical PropertiesBack Directory
[Melting point ]

150-154 °C (lit.)
[Boiling point ]

368.2±30.0 °C(Predicted)
[density ]

1.254±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[form ]

powder to crystal
[pka]

3.15±0.10(Predicted)
[color ]

White to Light yellow
[InChIKey]

GUOMINFEASCICM-UHFFFAOYSA-N
[CAS DataBase Reference]

52938-97-3(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn,Xi
[Risk Statements ]

R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37:Wear suitable protective clothing and gloves .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HS Code ]

2932190090
Spectrum DetailBack Directory
[Spectrum Detail]

5-PHENYL-2-FUROIC ACID(52938-97-3)MS
5-PHENYL-2-FUROIC ACID(52938-97-3)IR1
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

52938-97-3(sigmaaldrich)
[TCI AMERICA]

5-Phenyl-2-furancarboxylic Acid,>98.0%(LC)(T)(52938-97-3)
Hazard InformationBack Directory
[Synthesis]

5-PHENYL-2-FURALDEHYDE

13803-39-9

5-PHENYL-2-FUROIC ACID

52938-97-3

GENERAL METHODS: To a mixed solution of 5-(3-chlorophenyl)-2-furaldehyde (19a) (206 mg, 1.00 mmol) dissolved in tert-butanol (37.5 mL) and water (7.5 mL) was added sequentially NaH2PO4 (213 mg, 1.50 mmol), 2-methyl-2-butene (0.78 mL, 7.50 mmol) and NaClO2 (228 mg, 2.50 mmol). The reaction mixture was stirred at room temperature for 11 hours. After completion of the reaction, the volatile solvent was removed by distillation under reduced pressure and water and 1N hydrochloric acid were added. The mixture was extracted with ethyl acetate (EtOAc). The organic layers were combined, washed with saturated brine, dried over anhydrous magnesium sulfate (MgSO4) and concentrated under reduced pressure to give 5-phenyl-2-furoic acid (22a) (214 mg, 97% yield) as a white solid.

[References]

[1] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 21, p. 6384 - 6393,10
[2] Journal of Pharmaceutical Sciences, 1980, vol. 69, # 1, p. 107 - 110
[3] Patent: US2010/130556, 2010, A1. Location in patent: Page/Page column 25
[4] Bulletin of the Chemical Society of Japan, 1975, vol. 48, p. 491,494
[5] Heterocycles, 2014, vol. 89, # 2, p. 453 - 464
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