2-Oxopropyltriphenylphosphonium chloride
99%
- Product Code: 121926
Alias:
Acetonyl triphenylphosphine chloride
CAS:
1235-21-8
| Molecular Weight: | 354.81 g./mol | Molecular Formula: | C₂₁H₂₀ClOP |
|---|---|---|---|
| EC Number: | 214-974-1 | MDL Number: | MFCD00011813 |
| Melting Point: | 243-245 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature, sealed |
Product Description:
Used as a reagent in organic synthesis, particularly in the Wittig reaction, to convert carbonyl compounds into alkenes. It is valuable in the preparation of complex organic molecules, including pharmaceuticals and natural products. The compound acts as a precursor for generating ylides, which are essential intermediates in carbon-carbon bond formation. Its application extends to the development of fine chemicals and specialized materials, where precise control over molecular structure is required. Additionally, it is employed in research settings to study reaction mechanisms and explore new synthetic pathways.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 248-252 |
| Purity (Titration With Agno3) | 98.5-101.5 |
| Appearance | Colorless Liquid |
| Infrared Spectrum | Conforms To Structure |
| Solubility In Hot Water | With Slightly Turbid Solution |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 25.000 | 10-20 days | Ft50,207.34 |
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2-Oxopropyltriphenylphosphonium chloride
Used as a reagent in organic synthesis, particularly in the Wittig reaction, to convert carbonyl compounds into alkenes. It is valuable in the preparation of complex organic molecules, including pharmaceuticals and natural products. The compound acts as a precursor for generating ylides, which are essential intermediates in carbon-carbon bond formation. Its application extends to the development of fine chemicals and specialized materials, where precise control over molecular structure is required. Additionally, it is employed in research settings to study reaction mechanisms and explore new synthetic pathways.
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