1,4-Dithiane
≥97%
- Product Code: 87225
CAS:
505-29-3
| Molecular Weight: | 120.24 g./mol | Molecular Formula: | C₄H₈S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00006658 | |
| Melting Point: | 107-113 °C(lit.) | Boiling Point: | 200 °C(lit.) |
| Density: | 1.062 g/ml | Storage Condition: | 2-8°C, dry |
Product Description:
1,4-Dithiane is widely used in organic synthesis as a versatile building block, particularly in the preparation of complex molecules. Its cyclic structure with sulfur atoms makes it valuable for creating ligands in coordination chemistry, where it helps stabilize metal complexes. This compound is also employed in the synthesis of thioether-containing polymers, which are useful in materials science due to their unique properties. Additionally, 1,4-dithiane serves as a precursor in the production of pharmaceuticals and agrochemicals, where its sulfur atoms play a key role in enhancing biological activity. Its ability to act as a protecting group for carbonyl compounds further expands its utility in multi-step synthetic processes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off-White Powder or Crystals |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $82.64 |
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| 5.000 | 10-20 days | $261.22 |
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| 25.000 | 10-20 days | $1,037.81 |
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1,4-Dithiane
1,4-Dithiane is widely used in organic synthesis as a versatile building block, particularly in the preparation of complex molecules. Its cyclic structure with sulfur atoms makes it valuable for creating ligands in coordination chemistry, where it helps stabilize metal complexes. This compound is also employed in the synthesis of thioether-containing polymers, which are useful in materials science due to their unique properties. Additionally, 1,4-dithiane serves as a precursor in the production of pharmaceuticals and agrochemicals, where its sulfur atoms play a key role in enhancing biological activity. Its ability to act as a protecting group for carbonyl compounds further expands its utility in multi-step synthetic processes.
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