4'-n-Butylacetophenone, 97%, Thermo Scientific Chemicals
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4'-n-Butylacetophenone, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

4'-n-Butylacetophenone, 97%, Thermo Scientific Chemicals

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5 g
25 g
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Catalog number A15296.06
also known as A15296-06
Price (USD)/ Each
63.80
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Quantity:
5 g
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Price (USD)/ Each
63.80
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4'-n-Butylacetophenone, 97%, Thermo Scientific Chemicals
Catalog numberA15296.06
Price (USD)/ Each
63.80
-
Add to cart
Chemical Identifiers
CAS37920-25-5
IUPAC Name1-(4-butylphenyl)ethan-1-one
Molecular FormulaC12H16O
InChI KeyMQESVSITPLILCO-UHFFFAOYSA-N
SMILESCCCCC1=CC=C(C=C1)C(C)=O
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SpecificationsSpecification SheetSpecification Sheet
FormLiquid
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥96.0%
Identification (FTIR)Conforms
Refractive Index1.5170-1.5220 @ 20?C
4'-n-Butylacetophenone is used as an organic chemical synthesis 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
4′-n-Butylacetophenone is used as an organic chemical synthesis intermediate.

Solubility
Not miscible in water.

Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents, acids and bases.
RUO – Research Use Only

General References:

  1. Isabelle Kondolff; Henri Doucet; Maurice Santelli. Tetraphosphine/palladium catalysed Suzuki cross-coupling reactions of aryl halides with alkylboronic acids. Tetrahedron. 2004, 60,(17), 3813-3818.
  2. Phil Ho Lee; Sung Wook Lee; Kooyeon Lee. Pd-catalyzed carbonylative cross-coupling reactions by triorganoindiums: Highly efficient transfer of organic groups attached to indium under atmospheric pressure. Org. Lett. 2003, 5,(7), 1103-1106.