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Thermo Scientific Chemicals
Acetonyltriphenylphosphonium chloride, 99%
CAS: 1235-21-8 | C21H20ClOP | 354.81 g/mol
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Catalog number A14691.36
also known as A14691-36
Price (EUR)
379,00
Each
Quantity:
500 g
Price (EUR)
379,00
Each
Chemical Identifiers
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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Specifications
Specification Sheet
Specification SheetAssay (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.
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:
- 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