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N-Benzoyl-2-hydroxy-2-phenylethylamine

CAS# 111059-46-2

N-Benzoyl-2-hydroxy-2-phenylethylamine

Catalog No. BCN1622----Order now to get a substantial discount!

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N-Benzoyl-2-hydroxy-2-phenylethylamine: 5mg Please Inquire In Stock
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Quality Control of N-Benzoyl-2-hydroxy-2-phenylethylamine

Number of papers citing our products

Chemical structure

N-Benzoyl-2-hydroxy-2-phenylethylamine

3D structure

Chemical Properties of N-Benzoyl-2-hydroxy-2-phenylethylamine

Cas No. 111059-46-2 SDF Download SDF
PubChem ID 744627 Appearance Powder
Formula C15H15NO2 M.Wt 241.29
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name N-[(2R)-2-hydroxy-2-phenylethyl]benzamide
SMILES C1=CC=C(C=C1)C(CNC(=O)C2=CC=CC=C2)O
Standard InChIKey JZUOCQXDQFRPAF-AWEZNQCLSA-N
Standard InChI InChI=1S/C15H15NO2/c17-14(12-7-3-1-4-8-12)11-16-15(18)13-9-5-2-6-10-13/h1-10,14,17H,11H2,(H,16,18)/t14-/m0/s1
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 N-Benzoyl-2-hydroxy-2-phenylethylamine

The Oxytropis pseudoglandulosa

Biological Activity of N-Benzoyl-2-hydroxy-2-phenylethylamine

DescriptionStandard reference
In vitro

Study on the Chemical Constituents of Oxytropis falcata Bunge[Reference: WebLink]

Natural Product Research & Development;Apr2009, Vol. 21 Issue 2, p246


METHODS AND RESULTS:
The ethanol extract of the Oxytropis falcata Bunge was separated by column chromatography and Recrystallization to afford seven compounds.On the spectroscopic analysis,they were identified as N-benzoyl-2-phenylethylamine(1),N-cinnamoyl-2-phenylethylamine(2),N-Benzoyl-2-hydroxy-2-phenylethylamine(3),2′-hydroxy-4′-methoxychalcone(4),7-methoxyflavanone(5),5-hydroxy-7-methoxyflavanone(6).β-sitosterol(7).
CONCLUSIONS:
Compounds 1-3,5 and 6 were isolated from this plant for the first time.Compounds 4 and 5 showed significant cytotoxic activity against the SGC cell with IC50 values of 3.61 and 6.11 μg/mL respectively.

N-Benzoyl-2-hydroxy-2-phenylethylamine Dilution Calculator

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N-Benzoyl-2-hydroxy-2-phenylethylamine Molarity Calculator

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Preparing Stock Solutions of N-Benzoyl-2-hydroxy-2-phenylethylamine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.1444 mL 20.722 mL 41.4439 mL 82.8878 mL 103.6098 mL
5 mM 0.8289 mL 4.1444 mL 8.2888 mL 16.5776 mL 20.722 mL
10 mM 0.4144 mL 2.0722 mL 4.1444 mL 8.2888 mL 10.361 mL
50 mM 0.0829 mL 0.4144 mL 0.8289 mL 1.6578 mL 2.0722 mL
100 mM 0.0414 mL 0.2072 mL 0.4144 mL 0.8289 mL 1.0361 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 N-Benzoyl-2-hydroxy-2-phenylethylamine

Study on the Chemical Constituents of Oxytropis falcata Bunge

Natural Product Research & Development;Apr2009, Vol. 21 Issue 2, p246

The ethanol extract of the Oxytropis falcata Bunge was separated by column chromatography and Recrystallization to afford seven compounds.On the spectroscopic analysis,they were identified as N-benzoyl-2-phenylethylamine(1),N-cinnamoyl-2-phenylethylamine(2),N-Benzoyl-2-hydroxy-2-phenylethylamine(3),2′-hydroxy-4′-methoxychalcone(4),7-methoxyflavanone(5),5-hydroxy-7-methoxyflavanone(6).β-sitosterol(7).Compounds 1-3,5 and 6 were isolated from this plant for the first time.Compounds 4 and 5 showed significant cytotoxic activity against the SGC cell with IC50 values of 3.61 and 6.11 μg/mL respectively.

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