1,3-DITHIOLE-2-THIONE-4,5-DICARBOXYLIC ACID DIMETHYL ESTER
1,3-DITHIOLE-2-THIONE-4,5-DICARBOXYLIC ACID DIMETHYL ESTER Basic information
- Product Name:
- 1,3-DITHIOLE-2-THIONE-4,5-DICARBOXYLIC ACID DIMETHYL ESTER
- Synonyms:
-
- 1,3-DITHIOLE-2-THIONE-4,5-DICARBOXYLIC ACID DIMETHYL ESTER
- DIMETHYL 2-THIOXO-1,3-DITHIOLE-4,5-DICARBOXYLATE
- DIMETHYL 1,3-DITHIOLE-2-THIONE-4,5-DICARBOXYLATE
- 2-Thioxo-1,3-dithiole-4,5-dicarboxylic acid dimethyl ester
- Dimethyl 2-Thioxo-1,3-dithiole-4,5-dicarboxylate 1,3-Dithiole-2-thione-4,5-dicarboxylic Acid Dimethyl Ester
- 2-Thioxo-1,3-dithiole-4,5-dicarboxylic acid
- Dimethyl1,3-Dithiole-2-thione-4,5-dicarboxylate>
- 1,3-Dithiole-4,5-dicarboxylic acid, 2-thioxo-, 4,5-dimethyl ester
- CAS:
- 7396-41-0
- MF:
- C7H6O4S3
- MW:
- 250.32
- Product Categories:
-
- Charge Transfer Complexes (Synthetic Intermediates)
- Charge Transfer Complexes for Organic Metals
- Functional Materials
- Heterocyclic Building Blocks
- Others
- S-Containing
- Building Blocks
- Chemical Synthesis
- Heterocyclic Building Blocks
- Mol File:
- 7396-41-0.mol
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1,3-DITHIOLE-2-THIONE-4,5-DICARBOXYLIC ACID DIMETHYL ESTER Chemical Properties
- Melting point:
- 86-90 °C (lit.)
- Boiling point:
- 362.5±52.0 °C(Predicted)
- Density
- 1.57±0.1 g/cm3(Predicted)
- solubility
- almost transparency in hot Methanol
- form
- powder to crystal
- color
- Light yellow to Brown
- BRN
- 1288368
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Safety Information
- WGK Germany
- 3
- F
- 8-10-23
- HS Code
- 2934.99.4400
MSDS
- Language:English Provider:SigmaAldrich
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1,3-DITHIOLE-2-THIONE-4,5-DICARBOXYLIC ACID DIMETHYL ESTER Usage And Synthesis
Definition
ChEBI: 2-sulfanylidene-1,3-dithiole-4,5-dicarboxylic acid dimethyl ester is a heteroarene.
Synthesis Reference(s)
The Journal of Organic Chemistry, 47, p. 4000, 1982 DOI: 10.1021/jo00141a044
General Description
Dimethyl 2-thioxo-1,3-dithiole-4,5-dicarboxylate is a sulphur-containing heterocyclic building block. It has been reported to be formed during the reaction of 1,3-dithiolan-2-thiones with dimethyl acetylenedicarboxylate. It is formed as major product during the reaction of ethylene trithiocarbonate with dimethyl acetylenedicarboxylate.
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