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Ethyltriphenylphosphonium iodide, 98+%, Thermo Scientific Chemicals
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Catalog number A17533.36
also known as A17533-36
Price (USD)/ Each
333.65
Online exclusive
370.00 Save 36.35 (10%)
-
Quantity:
500 g
Price (USD)/ Each
333.65
Online exclusive
370.00 Save 36.35 (10%)
Ethyltriphenylphosphonium iodide, 98+%, Thermo Scientific Chemicals
Catalog numberA17533.36
Price (USD)/ Each
333.65
Online exclusive
370.00 Save 36.35 (10%)
-
Chemical Identifiers
CAS4736-60-1
IUPAC Nameethyltriphenylphosphanium iodide
Molecular FormulaC20H20IP
InChI KeySLAFUPJSGFVWPP-UHFFFAOYSA-M
SMILES[I-].CC[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetAssay (Titration ex Iodide)≥98.0 to ≤102.0%
Water Content (Karl Fischer Titration)≤1%
FormCrystals or powder or crystalline powder or fused solid
Appearance (Color)White to cream
Identification (FTIR)Conforms
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Ethyltriphenylphosphonium iodide is involved in synthesis of diarylmethine derivatives, phosphonium salts, and bismuth(III) polynuclear halide complexes, asymmetric hydrogenation.
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
Ethyltriphenylphosphonium iodide is involved in synthesis of diarylmethine derivatives, phosphonium salts, and bismuth(III) polynuclear halide complexes, asymmetric hydrogenation.
Solubility
Soluble in water.
Notes
Light Sensitive & Hygroscopic. Keep container tightly closed. Store away from oxidizing agents.
Ethyltriphenylphosphonium iodide is involved in synthesis of diarylmethine derivatives, phosphonium salts, and bismuth(III) polynuclear halide complexes, asymmetric hydrogenation.
Solubility
Soluble in water.
Notes
Light Sensitive & Hygroscopic. Keep container tightly closed. Store away from oxidizing agents.
RUO – Research Use Only
General References:
- Carl Michael Dicken.; Philip DeShong. Reactions at high pressures. [3+2] Dipolar cycloaddition of nitrones with vinyl ethers. J. Org. Chem. 1982, 47, (11), 2047-2051.
- Andrzej Robert Daniewski.; Jaroslaw Kiegiel. A simple way to (3aR,4S,7aS)-(Z)-ethylideneoctahydro-7a-methyl-1H-4-indenol, a synthon for total synthesis of vitamins D. J. Org. Chem. 1988, 53, (23), 5534-5535.
- The phosphorane, generated by reaction with n-BuLi, reacts with nitriles to give high yields of ketones: J. Am. Chem. Soc., 89, 7009 (1967).