(3-Ethoxy-3-oxopropyl)triphenylphosphonium bromide
97%
- Product Code: 69027
CAS:
42843-94-7
| Molecular Weight: | 443.31 g./mol | Molecular Formula: | C₂₃H₂₄BrO₂P |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03701355 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, inert gas atmosphere |
Product Description:
This compound is primarily utilized in organic synthesis as a reagent for the Wittig reaction, which is a key method for forming alkenes from aldehydes or ketones. It acts as a source of the ylide intermediate, enabling the conversion of carbonyl compounds into alkenes with high selectivity and efficiency. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, natural products, and fine chemicals. Additionally, its use in the preparation of conjugated polyenes and other unsaturated compounds is significant in materials science and polymer chemistry. The compound’s ability to facilitate carbon-carbon bond formation under mild conditions makes it a versatile tool in synthetic organic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿570.00 |
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| 1.000 | 10-20 days | ฿1,600.00 |
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| 5.000 | 10-20 days | ฿5,220.00 |
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| 25.000 | 10-20 days | ฿19,350.00 |
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| 100.000 | 10-20 days | ฿34,020.00 |
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(3-Ethoxy-3-oxopropyl)triphenylphosphonium bromide
This compound is primarily utilized in organic synthesis as a reagent for the Wittig reaction, which is a key method for forming alkenes from aldehydes or ketones. It acts as a source of the ylide intermediate, enabling the conversion of carbonyl compounds into alkenes with high selectivity and efficiency. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, natural products, and fine chemicals. Additionally, its use in the preparation of conjugated polyenes and other unsaturated compounds is significant in materials science and polymer chemistry. The compound’s ability to facilitate carbon-carbon bond formation under mild conditions makes it a versatile tool in synthetic organic chemistry.
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