1,2-Dichloro-3-iodobenzene
97%
- Product Code: 80509
Alias:
1, 2-Dichloro-3-iodobenzene
CAS:
2401-21-0
| Molecular Weight: | 272.9 g./mol | Molecular Formula: | Cl₂C₆H₃I |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00001034 | |
| Melting Point: | 35-36 °C(lit.) | Boiling Point: | 123-126 °C20 mm Hg(lit.) |
| Density: | Storage Condition: | room temperature, away from light |
Product Description:
1,2-Dichloro-3-iodobenzene is primarily utilized in organic synthesis as a versatile intermediate. Its structure allows for selective functionalization, making it valuable in the preparation of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create biaryl compounds or substituted aromatic systems. Additionally, it serves as a precursor in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. The presence of chlorine and iodine atoms enables further derivatization, enhancing its utility in constructing diverse organic frameworks. Its role in medicinal chemistry is notable, particularly in the development of compounds with potential biological activity.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 34-38 |
| PurityGC | 97-100 |
| APPEARANCE | White to tan solid |
| INFRARED SPECTRUM | Conforms to Structure |
| SOLUBILITY IN METHANOL | almost transparency |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿390.00 |
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| 25.000 | 10-20 days | ฿1,250.00 |
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| 100.000 | 10-20 days | ฿4,610.00 |
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1,2-Dichloro-3-iodobenzene
1,2-Dichloro-3-iodobenzene is primarily utilized in organic synthesis as a versatile intermediate. Its structure allows for selective functionalization, making it valuable in the preparation of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create biaryl compounds or substituted aromatic systems. Additionally, it serves as a precursor in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. The presence of chlorine and iodine atoms enables further derivatization, enhancing its utility in constructing diverse organic frameworks. Its role in medicinal chemistry is notable, particularly in the development of compounds with potential biological activity.
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