2-Bromo-4-iodophenol
96%
- Product Code: 61840
CAS:
133430-98-5
| Molecular Weight: | 298.90 g./mol | Molecular Formula: | C₆H₄BrIO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11870189 | |
| Melting Point: | 51℃ | Boiling Point: | 280±30°C at 760 mmHg |
| Density: | Storage Condition: | 2-8°C, away from light, dry, sealed |
Product Description:
Used primarily in organic synthesis, this compound serves as a versatile intermediate in the production of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs) due to its halogenated structure, which allows for further functionalization. Additionally, it is employed in material science for the creation of specialized polymers and coatings, where its unique properties enhance durability and performance. In research, it acts as a building block in the synthesis of various organic compounds, aiding in the study of chemical reactions and mechanisms. Its dual halogen substitution makes it a useful reagent in cross-coupling reactions, which are critical in constructing carbon-carbon bonds in advanced chemical synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,178.00 |
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| 0.250 | 10-20 days | ฿3,258.00 |
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| 1.000 | 10-20 days | ฿6,903.00 |
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2-Bromo-4-iodophenol
Used primarily in organic synthesis, this compound serves as a versatile intermediate in the production of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs) due to its halogenated structure, which allows for further functionalization. Additionally, it is employed in material science for the creation of specialized polymers and coatings, where its unique properties enhance durability and performance. In research, it acts as a building block in the synthesis of various organic compounds, aiding in the study of chemical reactions and mechanisms. Its dual halogen substitution makes it a useful reagent in cross-coupling reactions, which are critical in constructing carbon-carbon bonds in advanced chemical synthesis.
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