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Thermo Scientific Chemicals
4'-tert-Butylacetophenone, 98%
CAS: 943-27-1 | C12H16O | 176.259 g/mol
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化學識別
CAS943-27-1
IUPAC Name1-(4-tert-butylphenyl)ethan-1-one
Molecular FormulaC12H16O
InChI KeyUYFJYGWNYQCHOB-UHFFFAOYSA-N
SMILESCC(=O)C1=CC=C(C=C1)C(C)(C)C
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規格
規格表
規格表FormLiquid
Refractive Index1.5185-1.5225 @ 20?C
Assay (GC)≥97.5%
Appearance (Color)Clear colorless to pale yellow
4'-tert-Butylacetophenone is used in the synthesis of 2-pyridone derivatives.
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
4′-tert-Butylacetophenone is used in the synthesis of 2-pyridone derivatives.
Solubility
Soluble in alcohol. Insoluble in water.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
4′-tert-Butylacetophenone is used in the synthesis of 2-pyridone derivatives.
Solubility
Soluble in alcohol. Insoluble in water.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Mats Larhed.; Anders Hallberg. Microwave-Promoted Palladium-Catalyzed Coupling Reactions. J. Org. Chem. 1996, 61 (26), 9582-9584.
- Alain Schlatter.; Wolf-D. Woggon. Enantioselective Transfer Hydrogenation of Aliphatic Ketones Catalyzed by Ruthenium Complexes Linked to the Secondary Face of β-Cyclodextrin. Advanced Synthesis & Catalysis. 2008, 350 (7-8), 995-1000.