1,3-Dibromo-2-iodobenzene
98%
- Product Code: 58976
CAS:
19821-80-8
| Molecular Weight: | 361.80 g./mol | Molecular Formula: | C₆H₃Br₂I |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00192666 | |
| Melting Point: | 100° C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block for the construction of complex molecules. Its unique combination of halogen substituents allows for selective functionalization, making it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create advanced intermediates for pharmaceuticals and agrochemicals. Additionally, it serves as a precursor in the development of liquid crystals and organic electronic materials due to its ability to modify molecular structures for desired electronic properties. Its reactivity also makes it useful in research settings for studying halogen exchange mechanisms and designing novel organic compounds.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 97.5-100 |
| MELTING POINT | 98-102 |
| Infrared spectrum | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,280.00 |
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| 5.000 | 10-20 days | ฿5,020.00 |
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1,3-Dibromo-2-iodobenzene
This chemical is primarily utilized in organic synthesis as a versatile building block for the construction of complex molecules. Its unique combination of halogen substituents allows for selective functionalization, making it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create advanced intermediates for pharmaceuticals and agrochemicals. Additionally, it serves as a precursor in the development of liquid crystals and organic electronic materials due to its ability to modify molecular structures for desired electronic properties. Its reactivity also makes it useful in research settings for studying halogen exchange mechanisms and designing novel organic compounds.
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