(Z)-ISOPROPYL 3-IODOACRYLATE
98%
- Product Code: 123720
CAS:
1333154-26-9
| Molecular Weight: | 240.04 g./mol | Molecular Formula: | C₆H₉IO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30537663 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry, protected from light |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the construction of complex molecules. It serves as a valuable building block in the preparation of various acrylate derivatives, which are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Its iodine atom makes it a versatile intermediate for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of bioactive compounds, including those with potential antimicrobial or anticancer properties. The (Z)-configuration of the double bond is crucial for its reactivity and selectivity in stereospecific transformations.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Yellow Liquid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,020.00 |
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| 0.250 | 10-20 days | ฿11,700.00 |
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| 1.000 | 10-20 days | ฿23,400.00 |
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| 5.000 | 10-20 days | ฿66,690.00 |
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(Z)-ISOPROPYL 3-IODOACRYLATE
This chemical is primarily utilized in organic synthesis, particularly in the construction of complex molecules. It serves as a valuable building block in the preparation of various acrylate derivatives, which are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Its iodine atom makes it a versatile intermediate for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of bioactive compounds, including those with potential antimicrobial or anticancer properties. The (Z)-configuration of the double bond is crucial for its reactivity and selectivity in stereospecific transformations.
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