Angelidiol

CAS# 156009-77-7

Angelidiol

2D Structure

Catalog No. BCN7964----Order now to get a substantial discount!

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Quality Control of Angelidiol

3D structure

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Angelidiol

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Chemical Properties of Angelidiol

Cas No. 156009-77-7 SDF Download SDF
PubChem ID 134715205 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 (8S)-8-[(2R)-1,2-dihydroxypropan-2-yl]-8,9-dihydrofuro[2,3-h]chromen-2-one
SMILES CC(CO)(C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O
Standard InChIKey QWQZTILKTKQJTA-SMDDNHRTSA-N
Standard InChI InChI=1S/C14H14O5/c1-14(17,7-15)11-6-9-10(18-11)4-2-8-3-5-12(16)19-13(8)9/h2-5,11,15,17H,6-7H2,1H3/t11-,14+/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 Angelidiol

The root of Angelica sinensis

Protocol of Angelidiol

Structure Identification
Journal of Chinese Pharmaceutical Sciences, 1997, 6(4):221-224.

Further isolation of coumarin from Angelica pubescens Maxim f. Shan et Yuan.[Reference: WebLink]


METHODS AND RESULTS:
The roots and rhizomes of Angelica pubescens Maxim f. Shan et Yuan were extd. with 80% ethanol for 3 times. After removing the solvent under reduced pressure, the concd. material was suspended in H2O and extd. successively with CHCl3, EtOAc and n-BuOH. 9 Coumarin compds. were isolated and they were identified as columbianedin, osthol, bergapten , isoimperatorin, Angelidiol (I), nodakenetin (II), marmesinin (III), columbianin (IV) and meranzin hydrate (V).
CONCLUSIONS:
Among them compd. I was a new natural product and compds. II-V were isolated for the first time from this plant. [on SciFinder(R)] 9 Coumarin compds. were isolated and they were identified as columbianedin, osthol, bergapten , isoimperatorin, Angelidiol (I), nodakenetin (II), marmesinin (III), columbianin (IV) and meranzin hydrate (V). Among them compd. I was a new natural product and compds. II-V were isolated for the first time from this plant. [on SciFinder(R)]

Angelidiol Dilution Calculator

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Angelidiol Molarity Calculator

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Preparing Stock Solutions of Angelidiol

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 Angelidiol

Further isolation of coumarin from Angelica pubescens Maxim f. Shan et Yuan.

Journal of Chinese Pharmaceutical Sciences, 1997, 6(4):221-224.

The roots and rhizomes of Angelica pubescens Maxim f. Shan et Yuan were extd. with 80% ethanol for 3 times. After removing the solvent under reduced pressure, the concd. material was suspended in H2O and extd. successively with CHCl3, EtOAc and n-BuOH. 9 Coumarin compds. were isolated and they were identified as columbianedin, osthol, bergapten , isoimperatorin, Angelidiol (I), nodakenetin (II), marmesinin (III), columbianin (IV) and meranzin hydrate (V). Among them compd. I was a new natural product and compds. II-V were isolated for the first time from this plant. [on SciFinder(R)]

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