Chemistry:Ethylene trithiocarbonate
From HandWiki
| |
| Names | |
|---|---|
| Other names
1,3-dithiolane-2-thione
| |
| Identifiers | |
3D model (JSmol)
|
|
| ChemSpider | |
| EC Number |
|
PubChem CID
|
|
| UNII | |
| |
| |
| Properties | |
| C3H4S3 | |
| Molar mass | 136.25 g·mol−1 |
| Appearance | yellow solid |
| Melting point | 37 °C (99 °F; 310 K) |
| Boiling point | 95–105 °C (203–221 °F; 368–378 K) 0.01 torr |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Tracking categories (test):
Ethylene trithiocarbonate is an organosulfur compound with the formula C
2H
4S
2CS.[1] This yellow solid is prepared by alkylation of trithiocarbonate with 1,2-dibromoethane.[2] Ethylene trithiocarbonate is an intermediate in the synthesis of tetrathiafulvalene and its derivatives.[3]
References
- ↑ Fallah-Mehrjardi, Mehdi (2018). "Review of the organic trithiocarbonates synthesis". Monatshefte für Chemie - Chemical Monthly 149 (11): 1931–1944. doi:10.1007/s00706-018-2256-1.
- ↑ Lee, Albert W. M.; Chan, W. H.; Wong, H. C. (1988). "One Pot Phase Transfer Synthesis of Trithiocarbonates from Carbon Bisulphide and Alkyl Halides". Synthetic Communications 18 (13): 1531–1536. doi:10.1080/00397918808081310.
- ↑ Gorgues, Alain; Hudhomme, Piétrick; Sallé, Marc (2004). "Highly Functionalized Tetrathiafulvalenes: Riding along the Synthetic Trail from Electrophilic Alkynes". Chemical Reviews 104 (11): 5151–5184. doi:10.1021/cr0306485. PMID 15535646.
 |  |
