(Ethoxycarbonylmethyl)triphenylphosphonium chloride
97%
- Product Code: 68685
Alias:
(Carboethoxymethyl)triphenylphosphonium chloride；Ethyl (triphenylphosphonio)acetate chloride
CAS:
17577-28-5
| Molecular Weight: | 384.84 g./mol | Molecular Formula: | CH₃CH₂O₂CCH₂PC₆H₅₃Cl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00011746 | |
| Melting Point: | 120-123 °C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is widely utilized in organic synthesis, particularly in the Wittig reaction, where it serves as a key reagent for the formation of alkenes. It reacts with aldehydes or ketones to generate olefins, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the synthesis of fine chemicals and intermediates due to its ability to facilitate carbon-carbon bond formation. Its stability and reactivity under mild conditions make it a preferred choice in laboratory and industrial settings for constructing specific molecular architectures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿540.00 |
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| 25.000 | 10-20 days | ฿1,332.00 |
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(Ethoxycarbonylmethyl)triphenylphosphonium chloride
This compound is widely utilized in organic synthesis, particularly in the Wittig reaction, where it serves as a key reagent for the formation of alkenes. It reacts with aldehydes or ketones to generate olefins, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the synthesis of fine chemicals and intermediates due to its ability to facilitate carbon-carbon bond formation. Its stability and reactivity under mild conditions make it a preferred choice in laboratory and industrial settings for constructing specific molecular architectures.
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