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Thermo Scientific Chemicals
(Ethoxycarbonylmethyl)triphenylphosphonium bromide, 98+%
CAS: 1530-45-6 | C22H22BrO2P | 429.29 g/mol
化学物質識別子
CAS1530-45-6
IUPAC Name(2-ethoxy-2-oxoethyl)triphenylphosphanium bromide
Molecular FormulaC22H22BrO2P
InChI KeyVJVZPTPOYCJFNI-UHFFFAOYSA-M
SMILES[Br-].CCOC(=O)C[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)White to cream
FormPowder or crystalline powder
Assay (Titration ex Bromide)≥97.5% to ≤102.5%
Water Content (Karl Fischer Titration)<1.0%
(Ethoxycarbonylmethyl)triphenylphosphonium bromide, is used as a pharmaceutical intermediate.
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
(Ethoxycarbonylmethyl)triphenylphosphonium bromide, is used as a pharmaceutical intermediate.
Solubility
It is soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from Strong oxidizing agents, Strong bases.
(Ethoxycarbonylmethyl)triphenylphosphonium bromide, is used as a pharmaceutical intermediate.
Solubility
It is soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from Strong oxidizing agents, Strong bases.
RUO – Research Use Only
General References:
- R Alvarez-Sánchez.; D Basketter.; C Pease. Studies of chemical selectivity of hapten, reactivity, and skin sensitization potency. 3. Synthesis and studies on the reactivity toward model nucleophiles of the 13C. Chem. Res. Toxicol. 2003, 16, (5), 627-636.
- A Shaabani.; E Soleimani.; HR Khavasi.; RD Hoffmann. An isocyanide-based three-component reaction: synthesis of fully substituted N-alkyl-2-triphenylphosphoranylidene glutarimides. Tetrahedron Letters. 2006, 47, (31), 5493-5496.
- For reaction with trifluoroacetic anhydride and triethylamine, followed by pyrolysis as a route to perfluoroalkyl acetylenes, see: Org. Synth. Coll., 9, 436 (1998):