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Diethyl phenylthiomethylphosphonate, 96%, Thermo Scientific Chemicals
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Catalog number A13660.09
also known as A13660-09
Price (USD)/ Each
76.30
-
Quantity:
10 g
Price (USD)/ Each
76.30
Diethyl phenylthiomethylphosphonate, 96%, Thermo Scientific Chemicals
Catalog numberA13660.09
Price (USD)/ Each
76.30
-
Chemical Identifiers
CAS38066-16-9
IUPAC Namediethyl [(phenylsulfanyl)methyl]phosphonate
Molecular FormulaC11H17O3PS
InChI KeyFBUXEPJJFVDUFE-UHFFFAOYSA-N
SMILESCCOP(=O)(CSC1=CC=CC=C1)OCC
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to pale yellow
FormLiquid
Refractive Index1.5310-1.5370 @ 20?C
Assay (GC)≥95.0%
Diethyl phenylthiomethylphosphonate is used to produce Diethylphosphorylmethylphenylsulfoxid, Chemical reagents, pharmaceutical research, pharmaceutical intermediates.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Diethyl phenylthiomethylphosphonate is used to produce Diethylphosphorylmethylphenylsulfoxid, Chemical reagents, pharmaceutical research, pharmaceutical intermediates.
Solubility
Difficult to mix.
Notes
Store in cool, dry conditions in well sealed containers. Keep container tightly closed.
Diethyl phenylthiomethylphosphonate is used to produce Diethylphosphorylmethylphenylsulfoxid, Chemical reagents, pharmaceutical research, pharmaceutical intermediates.
Solubility
Difficult to mix.
Notes
Store in cool, dry conditions in well sealed containers. Keep container tightly closed.
RUO – Research Use Only
General References:
- Horner-Wadsworth-Emmons olefination (see Appendix 1) with carbonyl compounds gives enol thioethers, convertible to aldehydes: J. Chem. Soc., 1324 (1963). Compare Diethyl methyl thiomethyl phosphonate, L00579.
- For use in a synthesis of vinylphosphonates, in which the double bond is introduced by sulfoxide elimination, see: Synthesis, 917 (1982):