Identification | More | [Name]
3-Methoxythiophene | [CAS]
17573-92-1 | [Synonyms]
3-METHOXYTHIOPHENE METHYL 3-THIENYL ETHER Methoxythiophene,95% | [EINECS(EC#)]
-0 | [Molecular Formula]
C5H6OS | [MDL Number]
MFCD00043894 | [Molecular Weight]
114.17 | [MOL File]
17573-92-1.mol |
Chemical Properties | Back Directory | [Appearance]
Clear light brown liquid | [Melting point ]
49-50 °C(Solv: ethyl ether (60-29-7); ligroine (8032-32-4)) | [Boiling point ]
80-82 °C/65 mmHg (lit.) | [density ]
1.143 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.532(lit.)
| [Fp ]
121 °F
| [storage temp. ]
Flammables area | [form ]
Liquid | [color ]
Clear light brown | [Sensitive ]
Air Sensitive | [BRN ]
106404 | [LogP]
1.810 (est) | [CAS DataBase Reference]
17573-92-1(CAS DataBase Reference) | [NIST Chemistry Reference]
Thiophene, 3-methoxy-(17573-92-1) |
Safety Data | Back Directory | [Risk Statements ]
R10:Flammable. | [Safety Statements ]
S16:Keep away from sources of ignition-No smoking . S27:Take off immediately all contaminated clothing . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [RIDADR ]
UN 1993 3/PG 3
| [WGK Germany ]
3
| [F ]
13 | [HazardClass ]
3 | [PackingGroup ]
III | [HS Code ]
29339900 |
Hazard Information | Back Directory | [Chemical Properties]
Clear light brown liquid | [Uses]
3-Methoxythiophene, is a heterocyclic building block used for the synthesis of more complex compounds containing Thiophene moiety. It can also be used for the preparation of novel thiophenyl-methylene-9H-fluorene-based low bandgap polymers. | [Synthesis Reference(s)]
Synthetic Communications, 20, p. 213, 1990 DOI: 10.1080/00397919008052285 | [General Description]
3-Methoxythiophene is a thiophene. The intramolecular and intermolecular geometries of crystals of 3-methoxythiophene were studied. Spectroscopic studies of bipolarons derived from oligomerized 3-methoxythiophene in solution has been reported. The electropolymerization of 3-methoxythiophene on Pt and Fe electrodes in an aqueous micellar medium containing sodium dodecyl sulfate and 10-3M bithiophene has been reported. Thin polymer films of 3-methoxythiophene at the cathode in a direct current discharge have been prepared. |
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