(Methoxycarbonylmethyl)triphenylphosphonium bromide
98%
- Product Code: 122955
Alias:
Methoxyformylmethyltriphenylphosphonium bromide; (Methoxycarbonylmethyl)triphenylphosphonium bromide
CAS:
1779-58-4
| Molecular Weight: | 415.26 g./mol | Molecular Formula: | C₂₁H₂₀BrO₂P |
|---|---|---|---|
| EC Number: | 217-222-0 | MDL Number: | MFCD00011801 |
| Melting Point: | 165-170 °C (dec.)(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C, dry |
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 by reacting with aldehydes or ketones. It is particularly effective in the synthesis of α,β-unsaturated esters, which are important intermediates in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it can be employed in the preparation of complex organic molecules, including natural products, due to its ability to facilitate carbon-carbon bond formation. Its stability and reactivity make it a valuable tool in the development of novel compounds with potential applications in medicinal chemistry and materials science.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 153 Degree Celsius |
| Purity (%) | 98-100 |
| Solubility In Methanol | Almost Transparency |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿300.00 |
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| 25.000 | 10-20 days | ฿790.00 |
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| 100.000 | 10-20 days | ฿2,320.00 |
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| 500.000 | 10-20 days | ฿9,960.00 |
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(Methoxycarbonylmethyl)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 by reacting with aldehydes or ketones. It is particularly effective in the synthesis of α,β-unsaturated esters, which are important intermediates in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it can be employed in the preparation of complex organic molecules, including natural products, due to its ability to facilitate carbon-carbon bond formation. Its stability and reactivity make it a valuable tool in the development of novel compounds with potential applications in medicinal chemistry and materials science.
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