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4-Hydroxy-6-methylcoumarin

CAS# 13252-83-0

4-Hydroxy-6-methylcoumarin

Catalog No. BCN9800----Order now to get a substantial discount!

Product Name & Size Price Stock
4-Hydroxy-6-methylcoumarin: 5mg $12 In Stock
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Quality Control of 4-Hydroxy-6-methylcoumarin

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Chemical structure

4-Hydroxy-6-methylcoumarin

Chemical Properties of 4-Hydroxy-6-methylcoumarin

Cas No. 13252-83-0 SDF Download SDF
PubChem ID N/A Appearance Powder
Formula C10H8O3 M.Wt 176.1
Type of Compound Coumarins Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
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.

Biological Activity of 4-Hydroxy-6-methylcoumarin

DescriptionReference standards.

4-Hydroxy-6-methylcoumarin Dilution Calculator

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4-Hydroxy-6-methylcoumarin Molarity Calculator

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Preparing Stock Solutions of 4-Hydroxy-6-methylcoumarin

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.6786 mL 28.393 mL 56.7859 mL 113.5718 mL 141.9648 mL
5 mM 1.1357 mL 5.6786 mL 11.3572 mL 22.7144 mL 28.393 mL
10 mM 0.5679 mL 2.8393 mL 5.6786 mL 11.3572 mL 14.1965 mL
50 mM 0.1136 mL 0.5679 mL 1.1357 mL 2.2714 mL 2.8393 mL
100 mM 0.0568 mL 0.2839 mL 0.5679 mL 1.1357 mL 1.4196 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-Hydroxy-6-methylcoumarin

Synthesis of new chlorin e6 trimethyl and protoporphyrin IX dimethyl ester derivatives and their photophysical and electrochemical characterizations.[Pubmed:25171181]

Chemistry. 2014 Oct 13;20(42):13644-55.

In view of increasing demands for efficient photosensitizers for photodynamic therapy (PDT), we herein report the synthesis and photophysical characterizations of new chlorin e6 trimethyl ester and protoporphyrin IX dimethyl ester dyads as free bases and Zn(II) complexes. The synthesis of these molecules linked at the beta-pyrrolic positions to pyrano[3,2-c]coumarin, pyrano[3,2-c]quinolinone, and pyrano[3,2-c]naphthoquinone moieties was performed by using the domino Knoevenagel hetero Diels-Alder reaction. The alpha-methylenechromanes, alpha-methylenequinoline, and ortho-quinone methides were generated in situ from a Knoevenagel reaction of 4-hydroxycoumarin, 4-Hydroxy-6-methylcoumarin, 4-hydroxy-N-methylquinolinone, and 2-hydroxy-1,4-naphthoquinone, respectively, with paraformaldehyde in dioxane. All the dyads as free bases and as Zn(II) complexes were obtained in high yields. All new compounds were fully characterized by 1D and 2D NMR techniques, UV/Vis spectroscopy, and HRMS. Their photophysical properties were evaluated by measuring the fluorescence quantum yield, the singlet oxygen quantum yield by luminescence detection, and also the triplet lifetimes were correlated by flash photolysis and intersystem crossing (ISC) rates. The fluorescence lifetimes were measured by a time-correlated single photon count (TCSPC) method, fluorescence decay associated spectra (FDAS), and anisotropy measurements. Magnetic circular dichroism (MCD) and circular dichroism (CD) spectra were recorded for one Zn(II) complex in order to obtain information, respectively, on the electronic and conformational states, and interpretation of these spectra was enhanced by molecular orbital (MO) calculations. Electrochemical studies of the Zn(II) complexes were also carried out to gain insights into their behavior for such applications.

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