1,4-Diiodo-2,5-dimethylbenzene
98%
- Product Code: 78112
CAS:
1124-08-9
| Molecular Weight: | 357.95 g./mol | Molecular Formula: | C₈H₈I₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00829126 | |
| Melting Point: | 103-104°C | Boiling Point: | 306.2°C |
| Density: | 2.154g/mL | Storage Condition: | room temperature, dry |
Product Description:
1,4-Diiodo-2,5-dimethylbenzene is primarily used in organic synthesis as a building block for more complex chemical structures. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. The compound is particularly valuable in cross-coupling reactions, such as the Suzuki or Sonogashira reactions, where it helps form carbon-carbon bonds essential for creating advanced organic molecules. Additionally, its iodine atoms make it useful in the synthesis of liquid crystals and materials for organic electronics, including OLEDs. The compound’s stability and reactivity also make it a candidate for research in catalysis and polymer chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White - Almost white Crystal - Powder |
| PURITY | 97.5-100 |
| MELTING POINT | 102-106 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $117.08 |
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| 1.000 | 10-20 days | $209.22 |
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| 5.000 | 10-20 days | $713.90 |
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1,4-Diiodo-2,5-dimethylbenzene
1,4-Diiodo-2,5-dimethylbenzene is primarily used in organic synthesis as a building block for more complex chemical structures. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. The compound is particularly valuable in cross-coupling reactions, such as the Suzuki or Sonogashira reactions, where it helps form carbon-carbon bonds essential for creating advanced organic molecules. Additionally, its iodine atoms make it useful in the synthesis of liquid crystals and materials for organic electronics, including OLEDs. The compound’s stability and reactivity also make it a candidate for research in catalysis and polymer chemistry.
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