Acetonyltriphenylphosphonium chloride, 99%
Acetonyltriphenylphosphonium chloride, 99%
Acetonyltriphenylphosphonium chloride, 99%
Acetonyltriphenylphosphonium chloride, 99%
Thermo Scientific Chemicals

Acetonyltriphenylphosphonium chloride, 99%

CAS: 1235-21-8 | C21H20ClOP | 354.81 g/mol
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產品號碼 A14691.36
亦稱為 A14691-36
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500 g
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化學識別
CAS1235-21-8
IUPAC Name(2-oxopropyl)triphenylphosphanium chloride
Molecular FormulaC21H20ClOP
InChI KeyXAMZZEBAJZJERT-UHFFFAOYSA-M
SMILES[Cl-].CC(=O)C[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
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規格Specification Sheet規格表
Assay (Titration ex Chloride)≥98.5 to ≤101.5%
Appearance (Color)White to pale cream
Melting Point (clear melt)242.0-248.0?C
FormCrystals or powder or crystalline powder
Acetonyltriphenylphosphonium chloride is used to investigate the antimycobacterial activities of Me alkenyl quinolones. It is used as a reactant for synthesis of unsaturated esters and ketones containing multiple aromatic and heteroaromatic rings using Suzuki coupling - Wittig olefination.

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
Acetonyltriphenylphosphonium chloride is used to investigate the antimycobacterial activities of Me alkenyl quinolones. It is used as a reactant for synthesis of unsaturated esters and ketones containing multiple aromatic and heteroaromatic rings using Suzuki coupling - Wittig olefination.

Solubility
Soluble in hot water.

Notes
It is hygroscopic. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Abraham A.Wube; Antje Hufner; Christina Thomaschitz; Martina Blunder; Manfred Kollroser; Rudolf Bauer; Franz Bucar; Abraham A.Wube; Antje Hufner; Christina Thomaschitz; Martina Blunder; Manfred Kollroser; Rudolf Bauer; Franz Bucar. Design, synthesis and antimycobacterial activities of 1-methyl-2-alkenyl-4(1H)-quinolones. Bioorganic & Medicinal Chemistry. 2011, 19, (1),567-579