(Methoxymethyl)triphenylphosphonium chloride
98%
- Product Code: 113913
Alias:
(Methoxymethyl)triphenylphosphonium chloride; Methoxymethyltriphenylphosphonium chloride
CAS:
4009-98-7
Molecular Weight: | 342.8 g./mol | Molecular Formula: | C₂₀H₂₀ClOP |
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EC Number: | 223-664-5 | MDL Number: | MFCD00011800 |
Melting Point: | 185-195 °C (dec.)(lit.) | Boiling Point: | |
Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is widely used in organic synthesis as a reagent for the preparation of various organic compounds. It is particularly effective in the Wittig reaction, where it facilitates the formation of alkenes by reacting with aldehydes or ketones. This makes it valuable in the synthesis of complex molecules, including pharmaceuticals, agrochemicals, and natural products. Additionally, it is employed in the preparation of methoxymethyl ethers, which serve as protective groups for alcohols during multi-step synthetic processes. Its versatility and efficiency in these reactions make it a key tool in modern synthetic chemistry.
Product Specification:
Test | Specification |
---|---|
Purity (HPLC%) | 98-100 |
Melting Point (Degree Celsius) | 195-197 |
Purity (Titration With AgNO3) | 96.5-103.5 |
Appearance | White To Grey Powder Or Crystals |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | $15.07 |
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25.000 | 10-20 days | $20.59 |
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100.000 | 10-20 days | $43.19 |
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500.000 | 10-20 days | $203.92 |
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2500.000 | 10-20 days | $997.49 |
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(Methoxymethyl)triphenylphosphonium chloride
This chemical is widely used in organic synthesis as a reagent for the preparation of various organic compounds. It is particularly effective in the Wittig reaction, where it facilitates the formation of alkenes by reacting with aldehydes or ketones. This makes it valuable in the synthesis of complex molecules, including pharmaceuticals, agrochemicals, and natural products. Additionally, it is employed in the preparation of methoxymethyl ethers, which serve as protective groups for alcohols during multi-step synthetic processes. Its versatility and efficiency in these reactions make it a key tool in modern synthetic chemistry.
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