Methyl (triphenylphosphoranylidene)acetate

98%

  • Product Code: 122943
  Alias:    Methoxyformylmethylenetriphenylphosphine ; Methyl triphenylphosphorylidene acetate
  CAS:    2605-67-6
Molecular Weight: 334.35 g./mol Molecular Formula: C₂₁H₁₉O₂P
EC Number: 220-018-4 MDL Number: MFCD00008455
Melting Point: 168-172 °C(lit.) Boiling Point:
Density: Storage Condition: 2~8°C, away from light
Product Description: This chemical is widely used in organic synthesis, particularly in the Wittig reaction, where it serves as a key reagent for the formation of alkenes. It reacts with aldehydes and ketones to produce α,β-unsaturated esters, which are valuable intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is employed in the preparation of conjugated systems and complex organic molecules, making it a versatile tool in synthetic chemistry. Its stability and reactivity under mild conditions make it a preferred choice for constructing carbon-carbon double bonds in various research and industrial applications.
Product Specification:
Test Specification
Melting Point 164-172
Purity (%) 98-100
Triphenylphosphine And Triphenylphosphine Oxide (HPLC) 0-2
Triphenylphosphine And Triphenylphosphine Oxide (HPLC) 0-2
Appearance White To Off-White Crystalline Powder
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days Ft3,770.94
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25.000 10-20 days Ft6,679.95
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-
100.000 10-20 days Ft23,595.30
+
-
500.000 10-20 days Ft115,067.47
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Methyl (triphenylphosphoranylidene)acetate
This chemical is widely used in organic synthesis, particularly in the Wittig reaction, where it serves as a key reagent for the formation of alkenes. It reacts with aldehydes and ketones to produce α,β-unsaturated esters, which are valuable intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is employed in the preparation of conjugated systems and complex organic molecules, making it a versatile tool in synthetic chemistry. Its stability and reactivity under mild conditions make it a preferred choice for constructing carbon-carbon double bonds in various research and industrial applications.
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