Ethyltriphenylphosphonium iodide
95%
- Product Code: 121964
Alias:
Ethyltriphenylphosphine iodide
CAS:
4736-60-1
Molecular Weight: | 418.25 g./mol | Molecular Formula: | C₂₀H₂₀IP |
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EC Number: | 225-245-2 | MDL Number: | MFCD00040352 |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, away from light |
Product Description:
Ethyltriphenylphosphonium iodide is widely used as a phase-transfer catalyst in organic synthesis, facilitating reactions between compounds in different phases. It is particularly effective in nucleophilic substitution reactions, where it enhances the transfer of anions from the aqueous phase to the organic phase. This compound is also employed in the synthesis of phosphonium salts, which are valuable intermediates in the production of various organic compounds. Additionally, it finds application in the preparation of ylides, which are crucial in Wittig reactions for forming alkenes. Its role in promoting efficient and selective reactions makes it a valuable tool in both academic research and industrial chemistry.
Product Specification:
Test | Specification |
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Loss On Drying (%) | 0-1 |
Melting Point (Degree Celsius) | 164-169 |
Purity (Titration With AgNO3) (%) | 94.5-105.5 |
Appearance | White To Light Yellow Powder |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | ฿290.00 |
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25.000 | 10-20 days | ฿650.00 |
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100.000 | 10-20 days | ฿2,420.00 |
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Ethyltriphenylphosphonium iodide
Ethyltriphenylphosphonium iodide is widely used as a phase-transfer catalyst in organic synthesis, facilitating reactions between compounds in different phases. It is particularly effective in nucleophilic substitution reactions, where it enhances the transfer of anions from the aqueous phase to the organic phase. This compound is also employed in the synthesis of phosphonium salts, which are valuable intermediates in the production of various organic compounds. Additionally, it finds application in the preparation of ylides, which are crucial in Wittig reactions for forming alkenes. Its role in promoting efficient and selective reactions makes it a valuable tool in both academic research and industrial chemistry.
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