2-Chloro-6-(1,3-dithian-2-yl)pyrazine
95%
- Product Code: 94774
CAS:
874114-31-5
| Molecular Weight: | 232.75 g./mol | Molecular Formula: | C₈H₉ClN₂S₂ |
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| EC Number: | MDL Number: | MFCD22047071 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. Its unique structure, featuring a pyrazine ring and a 1,3-dithiane moiety, makes it valuable in the development of pharmaceuticals and agrochemicals. The compound is often employed in reactions where the dithiane group acts as a masked carbonyl equivalent, allowing for controlled transformations in multi-step synthesis. Additionally, its chloro-substituted pyrazine core is reactive in cross-coupling reactions, enabling the formation of carbon-carbon bonds for the creation of diverse heterocyclic compounds. This makes it particularly useful in the design of bioactive molecules and materials with specific functional properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $2,112.53 |
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2-Chloro-6-(1,3-dithian-2-yl)pyrazine
This chemical is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. Its unique structure, featuring a pyrazine ring and a 1,3-dithiane moiety, makes it valuable in the development of pharmaceuticals and agrochemicals. The compound is often employed in reactions where the dithiane group acts as a masked carbonyl equivalent, allowing for controlled transformations in multi-step synthesis. Additionally, its chloro-substituted pyrazine core is reactive in cross-coupling reactions, enabling the formation of carbon-carbon bonds for the creation of diverse heterocyclic compounds. This makes it particularly useful in the design of bioactive molecules and materials with specific functional properties.
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