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| 2-Iodothiophene Basic information |
| 2-Iodothiophene Chemical Properties |
Melting point | -40 °C (lit.) | Boiling point | 73 °C/15 mmHg (lit.) | density | 1.902 g/mL at 25 °C (lit.) | refractive index | n20/D 1.651(lit.) | Fp | 160 °F | storage temp. | 2-8°C | form | Liquid | Specific Gravity | 1.902 | color | Clear yellow-green to red-brown | Sensitive | Light Sensitive | BRN | 104666 | InChIKey | ROIMNSWDOJCBFR-UHFFFAOYSA-N | CAS DataBase Reference | 3437-95-4(CAS DataBase Reference) | NIST Chemistry Reference | Thiophene, 2-iodo-(3437-95-4) | EPA Substance Registry System | Thiophene, 2-iodo- (3437-95-4) |
| 2-Iodothiophene Usage And Synthesis |
Chemical Properties | colorless to light yellow liquid | Uses | 2-Iodothiophene was used in the synthesis of (E)-and (Z)-2,3-difluoro-3-aryl substituted acrylic esters. It was also used as monomer in the preparation of thin conductive films via plasma polymerization of 2-iodothiophene. | Synthesis Reference(s) | Tetrahedron Letters, 36, p. 4883, 1995 DOI: 10.1016/0040-4039(95)00876-E | General Description | Mechanism of the fluoride-free, palladium-catalyzed cross-coupling reaction of 2-iodothiophene with potassium (E)-heptenyldimethylsilanolate has been investigated. 2-Iodothiophene participates in microwave-enhanced, rapid homogeneous-phase version of the Sonogashira reaction. |
| 2-Iodothiophene Preparation Products And Raw materials |
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