Name | 3-DODECYLTHIOPHENE |
Synonyms | K0290 S1033 3-Laurylthiophene 3-DODECYLTHIOPHENE 3-N-LAURYLTHIOPHENE 3-N-DODECYLTHIOPHENE Thiophene,3-dodecyl- 1-(Thien-3-yl)dodecane 3-(Dodec-1-yl)thiophene |
CAS | 104934-52-3 |
InChI | InChI=1/C16H28S/c1-2-3-4-5-6-7-8-9-10-11-12-16-13-14-17-15-16/h13-15H,2-12H2,1H3 |
InChIKey | RFKWIEFTBMACPZ-UHFFFAOYSA-N |
Molecular Formula | C16H28S |
Molar Mass | 252.46 |
Density | 0.902 g/mL at 25 °C (lit.) |
Melting Point | -0.15°C (estimate) |
Boling Point | 290 °C (lit.) |
Flash Point | >230°F |
Vapor Presure | 0.000276mmHg at 25°C |
Appearance | clear liquid |
Color | Colorless to Light yellow |
Storage Condition | 2-8°C |
Refractive Index | n20/D 1.488(lit.) |
Physical and Chemical Properties | Storage Conditions: 0-6 ℃ WGK Germany:3 |
Safety Description | 24/25 - Avoid contact with skin and eyes. |
WGK Germany | 3 |
HS Code | 29339900 |
Overview | under N2 atmosphere, to contain magnesium dust (3.28g,0.135mol), anhydrous THF(30ml) A solution of 1-bromododecane (28.75g,26.9mL,0.13mol) in anhydrous THF(45mL) was added slowly to a mL three-necked flask with a small amount of iodine mixture. After the mixture was refluxed at 70 ° C. For 2 hours, the system was cooled to room temperature with ice water, and Ni(dppp)Cl2(0.54g, 1.00mmol) was added first, A solution of 3-bromothiophene (16.31g,0.10mol) in dry THF(40ml) was added slowly. The mixed solution was stirred overnight at room temperature and the reaction was quenched by the addition of cold aqueous HCl(1.50mol/L). The crude product was extracted with dichloromethane, dried over anhydrous magnesium sulfate, and further purified by chromatography column separation purification (n-hexane as eluent) to give a clear liquid (22.18g,88%). 1H NMR(300MHz,CDCl3): Δ7.22 (m,1H),6.95(m,2H),2.63(t,2H), 1.65(m,2H),1.32(m,18h),0.89(t,3H). |
Application | 3-dodecylthiophene is an organic intermediate, it can be prepared from 3-bromothiophene and halogenated hydrocarbon in one step and can be used to prepare photoelectric materials. |
Use | conductive polymer precursor |