Rutaretin

CAS# 13895-92-6

Rutaretin

Catalog No. BCN4710----Order now to get a substantial discount!

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Chemical structure

Rutaretin

3D structure

Chemical Properties of Rutaretin

Cas No. 13895-92-6 SDF Download SDF
PubChem ID 44146779 Appearance Powder
Formula C14H14O5 M.Wt 262.26
Type of Compound Coumarins Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (2S)-9-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one
SMILES CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O)O
Standard InChIKey FVFQELHSZVFPDZ-VIFPVBQESA-N
Standard InChI InChI=1S/C14H14O5/c1-14(2,17)9-6-8-5-7-3-4-10(15)19-12(7)11(16)13(8)18-9/h3-5,9,16-17H,6H2,1-2H3/t9-/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 Rutaretin

The herbs of Ruta graveolens L.

Biological Activity of Rutaretin

DescriptionStandard reference

Protocol of Rutaretin

Structure Identification
Tetrahedron.1981;37(2):285-290.

Studies on the chemical constituents of rutaceous plants—XLI : Absolute configuration of rutaretin methyl ether.[Reference: WebLink]


METHODS AND RESULTS:
The absolute configuration of Rutaretin methylether(1) has been established by transformation of it into methyl hexahydroRutaretin methyl ether (5) which was independently derived from S-marmesin (2) via photo-Fries reaction as a key step.

Nat Prod Res. 2004 Apr;18(2):141-6.

Marmenol: a 7-geranyloxycoumarin from the leaves of Aegle marmelos Corr.[Pubmed: 14984087 ]


METHODS AND RESULTS:
A new 7-geranyloxycoumarin [7-(2,6-dihydroxy-7-methoxy-7-methyl-3-octaenyloxy) coumarin] named marmenol (1) has been isolated from the leaves of methanolic extract of Aegle marmelos belonging to the family Rutaceae. In addition to marmenol, several known compounds have also been obtained for the first time from the same source. They include: praealtin D, trans-cinnamic acid, valencic acid, 4-methoxy benzoic acid, betulinic acid, N-p-cis- and trans-coumaroyltyramine, montanine, and Rutaretin.
CONCLUSIONS:
The structures of marmenol and known constituents were established with the help of NMR spectroscopy. However, structure of 1 was further confirmed via 2-D NMR experiments.

Rutaretin Dilution Calculator

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Rutaretin Molarity Calculator

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Preparing Stock Solutions of Rutaretin

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.813 mL 19.065 mL 38.1301 mL 76.2602 mL 95.3252 mL
5 mM 0.7626 mL 3.813 mL 7.626 mL 15.252 mL 19.065 mL
10 mM 0.3813 mL 1.9065 mL 3.813 mL 7.626 mL 9.5325 mL
50 mM 0.0763 mL 0.3813 mL 0.7626 mL 1.5252 mL 1.9065 mL
100 mM 0.0381 mL 0.1907 mL 0.3813 mL 0.7626 mL 0.9533 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 Rutaretin

Marmenol: a 7-geranyloxycoumarin from the leaves of Aegle marmelos Corr.[Pubmed:14984087]

Nat Prod Res. 2004 Apr;18(2):141-6.

A new 7-geranyloxycoumarin [7-(2,6-dihydroxy-7-methoxy-7-methyl-3-octaenyloxy) coumarin] named marmenol (1) has been isolated from the leaves of methanolic extract of Aegle marmelos belonging to the family Rutaceae. In addition to marmenol, several known compounds have also been obtained for the first time from the same source. They include: praealtin D, trans-cinnamic acid, valencic acid, 4-methoxy benzoic acid, betulinic acid, N-p-cis- and trans-coumaroyltyramine, montanine, and Rutaretin. The structures of marmenol and known constituents were established with the help of NMR spectroscopy. However, structure of 1 was further confirmed via 2-D NMR experiments.

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