4,5-Dichloro-1,2,3-dithiazol-1-ium chloride
95%
- Product Code: 87409
CAS:
75318-43-3
| Molecular Weight: | 208.52 g./mol | Molecular Formula: | C₂Cl₃NS₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03426194 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile reagent for the introduction of heterocyclic structures. It is particularly effective in the formation of dithiazole rings, which are valuable intermediates in the development of pharmaceuticals and agrochemicals. Its reactivity with various nucleophiles makes it a key component in the synthesis of complex molecules, including those with potential biological activity. Additionally, it is employed in the preparation of sulfur-containing compounds, which are crucial in materials science for creating polymers and other advanced materials. Its role in facilitating cyclization reactions also aids in the construction of diverse heterocyclic frameworks, enhancing the efficiency of synthetic routes in research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿315.00 |
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| 0.250 | 10-20 days | ฿648.00 |
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| 1.000 | 10-20 days | ฿1,845.00 |
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4,5-Dichloro-1,2,3-dithiazol-1-ium chloride
This chemical is primarily utilized in organic synthesis as a versatile reagent for the introduction of heterocyclic structures. It is particularly effective in the formation of dithiazole rings, which are valuable intermediates in the development of pharmaceuticals and agrochemicals. Its reactivity with various nucleophiles makes it a key component in the synthesis of complex molecules, including those with potential biological activity. Additionally, it is employed in the preparation of sulfur-containing compounds, which are crucial in materials science for creating polymers and other advanced materials. Its role in facilitating cyclization reactions also aids in the construction of diverse heterocyclic frameworks, enhancing the efficiency of synthetic routes in research and industrial applications.
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