2-Iodo-4-methoxy-1-(methylsulfonyl)benzene
97%
- Product Code: 116991
CAS:
1965309-05-0
| Molecular Weight: | 312.13 g./mol | Molecular Formula: | C₈H₉IO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30181850 | |
| Melting Point: | Boiling Point: | 419.8±45.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed away from light |
Product Description:
2-Iodo-4-methoxy-1-(methylsulfonyl)benzene is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring both iodo and methoxy groups, makes it a valuable building block in the development of more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create biaryl compounds or alkynylated derivatives. Additionally, the methylsulfonyl group enhances its reactivity, making it suitable for nucleophilic substitution reactions. This chemical is also explored in pharmaceutical research for the synthesis of potential drug candidates, particularly in the development of compounds with biological activity. Its utility extends to material science, where it contributes to the creation of advanced organic materials with specific electronic or optical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $65.08 |
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| 0.250 | 10-20 days | $92.62 |
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| 1.000 | 10-20 days | $222.23 |
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2-Iodo-4-methoxy-1-(methylsulfonyl)benzene
2-Iodo-4-methoxy-1-(methylsulfonyl)benzene is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring both iodo and methoxy groups, makes it a valuable building block in the development of more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create biaryl compounds or alkynylated derivatives. Additionally, the methylsulfonyl group enhances its reactivity, making it suitable for nucleophilic substitution reactions. This chemical is also explored in pharmaceutical research for the synthesis of potential drug candidates, particularly in the development of compounds with biological activity. Its utility extends to material science, where it contributes to the creation of advanced organic materials with specific electronic or optical properties.
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