Ethyl 4-ethyl-3-iodobenzoate
≥98%
- Product Code: 83848
CAS:
1131588-09-4
| Molecular Weight: | 304.12 g./mol | Molecular Formula: | C₁₁H₁₃IO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11112910 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Ethyl 4-ethyl-3-iodobenzoate is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring both an ethyl ester group and an iodine substituent, makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings. These reactions are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the compound can serve as a building block for the synthesis of complex organic molecules, particularly in medicinal chemistry, where it may contribute to the creation of drug candidates or biologically active compounds. Its iodine atom also allows for easy modification or labeling in research applications.
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 |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,690.00 |
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| 1.000 | 10-20 days | ฿9,070.00 |
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| 5.000 | 10-20 days | ฿28,800.00 |
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Ethyl 4-ethyl-3-iodobenzoate
Ethyl 4-ethyl-3-iodobenzoate is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring both an ethyl ester group and an iodine substituent, makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings. These reactions are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the compound can serve as a building block for the synthesis of complex organic molecules, particularly in medicinal chemistry, where it may contribute to the creation of drug candidates or biologically active compounds. Its iodine atom also allows for easy modification or labeling in research applications.
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