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| | 2,3-Dihydrofuran Basic information |
| Product Name: | 2,3-Dihydrofuran | | Synonyms: | 4,5-Dihydrofuran;2,3-dihydrofuran stab.;2 3-DIHYDROFURAN 99+%;2,3-DIHYDROFURANE;2,3-Dihydrofuran, 98+%;Furan, 2,3-dihydro-;2,3-Dihydrofuran,2,3-DHF;2,3-Dihydrofuran, 98+% 100GR | | CAS: | 1191-99-7 | | MF: | C4H6O | | MW: | 70.09 | | EINECS: | 214-747-7 | | Product Categories: | (intermediate of etodolac);Heterocycles, Intermediates, Metabolites & Impurities;Pyridines | | Mol File: | 1191-99-7.mol |  |
| | 2,3-Dihydrofuran Chemical Properties |
| Melting point | 280 °C(Solv: trichloroethylene (79-01-6); ethanol (64-17-5)) | | Boiling point | 54-55 °C (lit.) | | density | 0.927 g/mL at 25 °C (lit.) | | vapor pressure | 14.46 psi ( 55 °C) | | refractive index | n20/D 1.423(lit.) | | Fp | −12 °F | | storage temp. | 2-8°C | | solubility | soluble in Chloroform | | form | Liquid | | color | Clear colorless | | Water Solubility | slightly soluble | | BRN | 103168 | | InChIKey | JKTCBAGSMQIFNL-UHFFFAOYSA-N | | LogP | -0.034 (est) | | CAS DataBase Reference | 1191-99-7(CAS DataBase Reference) | | NIST Chemistry Reference | Furan, 2,3-dihydro-(1191-99-7) | | EPA Substance Registry System | Furan, 2,3-dihydro- (1191-99-7) |
| | 2,3-Dihydrofuran Usage And Synthesis |
| Chemical Properties | clear colourless liquid | | Uses | 2,3-Dihydrofuran is a dehydration product of tetrahydrofuran (THF). 2,3-Dihydrofuran is also used in the preparation of niologically active compounds such as antitumor agents. | | Uses | 2,3-Dihydrofuran is a versatile reagent used in lanthanide-catalyzed Diels-Alder reactions with 2-pyrones and in Rh(II)-stabilized cycloadditions with vinylcarbenoids. It is applied for alkylation by active methylene compounds, catalyzed by trans-Dichlorobis(triphenyl-phosphine)-palladium(II). It is also used in the preparation of biologically active compounds such as antitumor agents. | | Definition | ChEBI: 2,3-dihydrofuran is a dihydrofuran. | | General Description | The enantioselective Heck arylation of 2,3-dihydrofuran with aryl iodides was studied. |
| | 2,3-Dihydrofuran Preparation Products And Raw materials |
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