ChemicalBook--->CAS DataBase List--->17113-33-6

17113-33-6

17113-33-6 Structure

17113-33-6 Structure
IdentificationBack Directory
[Name]

2-PHENYL-FURAN
[CAS]

17113-33-6
[Synonyms]

2-PHENYL-FURAN
Furan, 2-phenyl-
[Molecular Formula]

C10H8O
[MDL Number]

MFCD00234628
[MOL File]

17113-33-6.mol
[Molecular Weight]

144.17
Chemical PropertiesBack Directory
[Melting point ]

161 °C
[Boiling point ]

222.78°C (rough estimate)
[density ]

1.0830
[refractive index ]

1.5920 (estimate)
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

Chloroform (Slightly), DMSO (Slightly)
[form ]

Oil
[color ]

Red to Dark Orange
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Questions And AnswerBack Directory
[Application]

2-Phenyran is a substituted furan. Furans are widely used oxygen-containing five-membered heterocyclic compounds, representing an important class of molecular structures. This structure is widely found in natural products and drug molecules, often serving as a building block in the synthesis of many complex heterocyclic compounds. There are many homologues of furan, and these products have wide applications, primarily as raw materials for novel pharmaceuticals, pesticides, fragrances, and chemical auxiliaries. In recent years, in particular, many novel drugs containing furan rings have been developed abroad, showing promising development prospects.
Hazard InformationBack Directory
[Synthesis Reference(s)]

The Journal of Organic Chemistry, 56, p. 3493, 1991 DOI: 10.1021/jo00011a010
Synthesis, p. 51, 1987
[Synthesis]

To a dry reaction flask was added dichloroditritophenylphosphine palladium (14 mg, 0.02 mmol), cuprous iodide (1.9 mg, 0.01 mmol), triethylamine (2 ml), iodobenzene (204 mg, 1 mmol), and 3-butyn-1-ol (84 mg, 1.2 mmol), and the reaction was carried out for
Spectrum DetailBack Directory
[Spectrum Detail]

2-PHENYL-FURAN(17113-33-6)1HNMR
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