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| Name = 1,2-Ethanedithiol | | Name = 1,2-Ethanedithiol | ||
| ImageFile = Ethanedithiol.png | | ImageFile = Ethanedithiol.png | ||
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| OtherNames = Dimercaptoethane<br />1,2-Ethanedithiol | | OtherNames = Dimercaptoethane<br />1,2-Ethanedithiol | ||
| Section1 = {{Chembox Identifiers | | Section1 = {{Chembox Identifiers | ||
| UNII_Ref = {{fdacite|correct|FDA}} | |||
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| UNII = 92T634FLAR | ||
| SMILES = SCCS | | SMILES = SCCS | ||
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
Revision as of 13:12, 6 August 2011
Names | |
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IUPAC name Ethane-1,2-dithiol | |
Other names
Dimercaptoethane 1,2-Ethanedithiol | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.007.958 |
RTECS number |
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UNII | |
CompTox Dashboard (EPA) | |
InChI
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SMILES
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Properties | |
Chemical formula | C2H6S2 |
Molar mass | 94.19 g·mol |
Appearance | Colorless liquid |
Density | 1.123 g/cm³ |
Melting point | −41 °C (−42 °F; 232 K) |
Boiling point | 146 °C (295 °F; 419 K) |
Solubility in water | Slightly sol |
Solubility in other solvents | Good solubility in most organic solvents |
Acidity (pKa) | ~11 |
Refractive index (nD) | 1.5589 (D-line, 25 °C) |
Hazards | |
NFPA 704 (fire diamond) | 2 2 |
Flash point | 50 °C |
Related compounds | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
1,2-Ethanedithiol is a colorless liquid with the formula C2H4(SH)2. It has a very characteristic odor which is compared by many people to rotten cabbage. It is a common building block in organic synthesis and an excellent ligand for metal ions.
Preparation
1,2-Ethanedithiol is commercially available. It can be prepared by the action of 1,2-dibromoethane on thiourea followed by hydrolysis.
Applications
This compound is widely used in organic chemistry because it reacts with aldehydes and ketones to give 1,3-dithiolanes, which are useful intermediates.
- C2H4(SH)2 + RR'CO → C2H4S2CRR' + H2O
Other 1,2- and 1,3-dithiols undergo this reaction to give related 1,3-dithiolanes and 1,3-dithianes (six-membered rings). Diols such as ethylene glycol undergo analogous reactions to 1,3-dioxalanes and 1,3-dioxanes. One distinguishing feature of the dithiolanes and dithianes derived from aldehydes is that the methyne group can be deprotonated and the resulting carbanion alkylated.
References
- Speziale, A. J. (1963). "Ethanedithiol". Organic Syntheses; Collected Volumes, vol. 4, p. 401.
- R. E. Conrow "Ethanedithiol" in Encyclopedia of Reagents for Organic Synthesis (Ed: L. Paquette) 2004, J. Wiley & Sons, New York. doi:10.1002/047084289