(R)-1-(4-Iodo-5-methoxy-2-nitrophenyl)-2,2-dimethylpropan-1-ol
≥95%
- Product Code: 113452
CAS:
1956436-50-2
| Molecular Weight: | 365.16 g./mol | Molecular Formula: | C₁₂H₁₆INO₄ |
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| EC Number: | MDL Number: | MFCD29916981 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of complex molecules. Its structure, featuring an iodine atom and nitro group, makes it particularly useful in coupling reactions, such as Suzuki or Sonogashira reactions, which are essential for constructing carbon-carbon bonds in pharmaceuticals and advanced materials. Additionally, the presence of a chiral center allows it to be employed in the synthesis of enantiomerically pure compounds, which are critical in drug development to ensure specificity and efficacy. The methoxy group further enhances its reactivity and selectivity in various chemical transformations, making it a versatile building block in medicinal chemistry and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿927.00 |
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| 0.250 | 10-20 days | ฿1,845.00 |
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(R)-1-(4-Iodo-5-methoxy-2-nitrophenyl)-2,2-dimethylpropan-1-ol
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of complex molecules. Its structure, featuring an iodine atom and nitro group, makes it particularly useful in coupling reactions, such as Suzuki or Sonogashira reactions, which are essential for constructing carbon-carbon bonds in pharmaceuticals and advanced materials. Additionally, the presence of a chiral center allows it to be employed in the synthesis of enantiomerically pure compounds, which are critical in drug development to ensure specificity and efficacy. The methoxy group further enhances its reactivity and selectivity in various chemical transformations, making it a versatile building block in medicinal chemistry and material science.
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