(Carbethoxyethylidene)triphenylphosphorane
96%
- Product Code: 121977
Alias:
Ethoxyformyl ethylenetriphenylphosphine; (1-ethoxycarbonyl acetal) triphenylphosphine bromide
CAS:
5717-37-3
| Molecular Weight: | 362.4 g./mol | Molecular Formula: | C₂₃H₂₃O₂P |
|---|---|---|---|
| EC Number: | 227-215-4 | MDL Number: | MFCD00009160 |
| Melting Point: | 158-162 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This chemical is primarily utilized in organic synthesis as a Wittig reagent, which is instrumental in the formation of alkenes through the reaction with aldehydes or ketones. Its application is particularly valuable in the synthesis of complex organic molecules, including pharmaceuticals and natural products, where it facilitates the introduction of carbon-carbon double bonds with high selectivity and efficiency. Additionally, it is employed in the preparation of conjugated systems, which are crucial in the development of materials with specific optical and electronic properties, such as organic semiconductors and light-emitting diodes (LEDs). The reagent's ability to generate stable ylides makes it a preferred choice in various synthetic pathways, contributing to advancements in medicinal chemistry and material science.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 158-163 |
| Purity (HPLC) | 98-100 |
| Appearance | Yellow Powder Or Crystals |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $14.09 |
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| 25.000 | 10-20 days | $24.42 |
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| 100.000 | 10-20 days | $78.43 |
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| 500.000 | 10-20 days | $387.92 |
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(Carbethoxyethylidene)triphenylphosphorane
This chemical is primarily utilized in organic synthesis as a Wittig reagent, which is instrumental in the formation of alkenes through the reaction with aldehydes or ketones. Its application is particularly valuable in the synthesis of complex organic molecules, including pharmaceuticals and natural products, where it facilitates the introduction of carbon-carbon double bonds with high selectivity and efficiency. Additionally, it is employed in the preparation of conjugated systems, which are crucial in the development of materials with specific optical and electronic properties, such as organic semiconductors and light-emitting diodes (LEDs). The reagent's ability to generate stable ylides makes it a preferred choice in various synthetic pathways, contributing to advancements in medicinal chemistry and material science.
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