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4-Phenylbutan-2-one

CAS# 2550-26-7

4-Phenylbutan-2-one

Catalog No. BCN3808----Order now to get a substantial discount!

Product Name & Size Price Stock
4-Phenylbutan-2-one: 5mg $23 In Stock
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Quality Control of 4-Phenylbutan-2-one

Number of papers citing our products

Chemical structure

4-Phenylbutan-2-one

3D structure

Chemical Properties of 4-Phenylbutan-2-one

Cas No. 2550-26-7 SDF Download SDF
PubChem ID 17355 Appearance Oil
Formula C10H12O M.Wt 148.2
Type of Compound Phenols Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 4-phenylbutan-2-one
SMILES CC(=O)CCC1=CC=CC=C1
Standard InChIKey AKGGYBADQZYZPD-UHFFFAOYSA-N
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of 4-Phenylbutan-2-one

The herbs of Dendrobium superbum

Biological Activity of 4-Phenylbutan-2-one

Description4-Phenylbutan-2-one is a model compound for the preparation of fragrances.

Protocol of 4-Phenylbutan-2-one

Structure Identification
Phys Chem Chem Phys. 2011 Aug 14;13(30):13579-84.

A smart palladium catalyst in ionic liquid for tandem processes.[Pubmed: 21750802 ]


METHODS AND RESULTS:
New catalytic systems based on in situ and preformed palladium nanoparticles in ionic liquids (characterised by TEM) starting from palladium acetate or dipalladiumtris(dibenzylideneacetone) have been applied in the synthesis of 4-Phenylbutan-2-one (II), a model compound for the preparation of fragrances. Imidazolium-based ionic liquid containing a methyl hydrogenophosphonate anion leads to an efficient Pd-catalyzed tandem coupling/reduction process, taking advantage of the multi-role of this solvent (nanoparticles stabiliser, base, hydrogen transfer agent). The influence of the mono-phosphine ligands (1-3) on the catalyst has been evaluated, showing that the ligand-free palladium system turns into the most appropriate for the formation of II using Pd(OAc)(2) as precursor.
CONCLUSIONS:
Fine-tuning conditions involved in this multi-parameter process have led us to propose a plausible mechanism based on the hydrogen transfer coming from the methyl hydrogenophosphonate anion.

4-Phenylbutan-2-one Dilution Calculator

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4-Phenylbutan-2-one Molarity Calculator

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Preparing Stock Solutions of 4-Phenylbutan-2-one

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 6.7476 mL 33.7382 mL 67.4764 mL 134.9528 mL 168.691 mL
5 mM 1.3495 mL 6.7476 mL 13.4953 mL 26.9906 mL 33.7382 mL
10 mM 0.6748 mL 3.3738 mL 6.7476 mL 13.4953 mL 16.8691 mL
50 mM 0.135 mL 0.6748 mL 1.3495 mL 2.6991 mL 3.3738 mL
100 mM 0.0675 mL 0.3374 mL 0.6748 mL 1.3495 mL 1.6869 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on 4-Phenylbutan-2-one

A smart palladium catalyst in ionic liquid for tandem processes.[Pubmed:21750802]

Phys Chem Chem Phys. 2011 Aug 14;13(30):13579-84.

New catalytic systems based on in situ and preformed palladium nanoparticles in ionic liquids (characterised by TEM) starting from palladium acetate or dipalladiumtris(dibenzylideneacetone) have been applied in the synthesis of 4-Phenylbutan-2-one (II), a model compound for the preparation of fragrances. Imidazolium-based ionic liquid containing a methyl hydrogenophosphonate anion leads to an efficient Pd-catalyzed tandem coupling/reduction process, taking advantage of the multi-role of this solvent (nanoparticles stabiliser, base, hydrogen transfer agent). The influence of the mono-phosphine ligands (1-3) on the catalyst has been evaluated, showing that the ligand-free palladium system turns into the most appropriate for the formation of II using Pd(OAc)(2) as precursor. Fine-tuning conditions involved in this multi-parameter process have led us to propose a plausible mechanism based on the hydrogen transfer coming from the methyl hydrogenophosphonate anion.

Description

Benzylacetone is an aromatic compound from agarwood. Benzylacetone exhibits potent and reversible antityrosinase (mushroom) activity, with IC50s of 2.8 mM and 0.6 mM for monophenolase and diphenolase, respectively. Benzylacetone has appetite-enhancing and locomotor-reducing effects.

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