Methyl 2-(triphenylphosphoranylidene)propanoate
95%
- Product Code: 41856
CAS:
2605-68-7
| Molecular Weight: | 348.38 g./mol | Molecular Formula: | C₂₂H₂₁O₂P |
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| EC Number: | MDL Number: | MFCD08062441 | |
| Melting Point: | Boiling Point: | 485.8±28.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the Wittig reaction, where it serves as a key reagent for the formation of alkenes. It facilitates the conversion of aldehydes and ketones into olefins, making it valuable in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and fine chemicals. Its ability to create carbon-carbon double bonds with high selectivity and efficiency is crucial in the development of compounds with specific stereochemistry. Additionally, it is employed in the synthesis of natural products and materials science for constructing polymers and advanced materials. Its stability and reactivity make it a versatile tool in synthetic chemistry laboratories.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $35.88 |
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| 0.250 | 10-20 days | $82.60 |
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| 1.000 | 10-20 days | $137.92 |
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| 5.000 | 10-20 days | $336.01 |
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Methyl 2-(triphenylphosphoranylidene)propanoate
This chemical is primarily used in organic synthesis, particularly in the Wittig reaction, where it serves as a key reagent for the formation of alkenes. It facilitates the conversion of aldehydes and ketones into olefins, making it valuable in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and fine chemicals. Its ability to create carbon-carbon double bonds with high selectivity and efficiency is crucial in the development of compounds with specific stereochemistry. Additionally, it is employed in the synthesis of natural products and materials science for constructing polymers and advanced materials. Its stability and reactivity make it a versatile tool in synthetic chemistry laboratories.
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