1,2-BENZENEDITHIOL
1,2-BENZENEDITHIOL Basic information
- Product Name:
- 1,2-BENZENEDITHIOL
- Synonyms:
-
- 1,2-BENZENEDITHIOL
- 1,2-DIMERCAPTOBENZENE
- 1,2-DIMERCAPTOBENZOL
- BENZOL-1,2-DITHIOL
- BENZENE-1,2-DITHIOL
- DITHIOCATECHOL
- 1,2-Benzenedithiol(9CI)
- 1,2-Benzenebisthiol
- CAS:
- 17534-15-5
- MF:
- C6H6S2
- MW:
- 142.24
- EINECS:
- 241-530-4
- Product Categories:
-
- THIOL
- Charge Transfer Complexes (Synthetic Intermediates)
- Charge Transfer Complexes for Organic Metals
- Functional Materials
- Sulfur Compounds (for Synthesis)
- Synthetic Organic Chemistry
- Mol File:
- 17534-15-5.mol
1,2-BENZENEDITHIOL Chemical Properties
- Melting point:
- 22-24 °C(lit.)
- Boiling point:
- 119-120 °C17 mm Hg(lit.)
- Density
- 1.236 g/mL at 25 °C(lit.)
- refractive index
- 1.6565-1.6585
- Flash point:
- 219 °F
- storage temp.
- 2-8°C
- solubility
- water: slightly soluble
- form
- Liquid After Melting
- pka
- 5.90±0.43(Predicted)
- Specific Gravity
- 1.236
- color
- Clear light yellow
- Water Solubility
- Soluble in water, benzene, ethanol, diethyl ether, ethyl acetate.
- Sensitive
- Air Sensitive
- BRN
- 636154
- CAS DataBase Reference
- 17534-15-5(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
1,2-BENZENEDITHIOL Usage And Synthesis
Chemical Properties
clear light yellow liquid after melting
Uses
1,2-Benzenedithiol is used in preparation of schiff base, which is employed to make new series of copper(II) and zinc(II) complexes.
Synthesis Reference(s)
Synthesis, p. 471, 1976 DOI: 10.1055/s-1976-24088
General Description
The transition metal complexes with benzene-1,2-dithiol as ligand were studied by UV-vis, resonance Raman (rR) and infrared (IR) spectroscopies.
Purification Methods
Likely impurities are the oxidation products, the disulfides which could be polymeric. Dissolve it in aqueous NaOH until the solution is alkaline. Extract with Et2O and discard the extract. Acidify with cold HCl (diluted 1:1 by volume with H2O) to Congo Red paper under N2 and extract it three times with Et2O. Dry the Et2O with Na2SO4, filter, evaporate and distil the residue under reduced pressure in an atmosphere of N2. The distillate solidifies on cooling. [UV: Dewar et al. J Chem Soc 3076 1958, Grunwald & Berkowitz J Am Chem Soc 81 4939 1951, Ferretti Org Synth Coll Vol V 419 1973, Beilstein 6 IV 5651.]
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