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Isosalvipuberulin

CAS# 115321-32-9

Isosalvipuberulin

Catalog No. BCN6030----Order now to get a substantial discount!

Product Name & Size Price Stock
Isosalvipuberulin:5mg Please Inquire In Stock
Isosalvipuberulin:10mg Please Inquire In Stock
Isosalvipuberulin:20mg Please Inquire In Stock
Isosalvipuberulin:50mg Please Inquire In Stock

Quality Control of Isosalvipuberulin

Number of papers citing our products

Chemical structure

Isosalvipuberulin

3D structure

Chemical Properties of Isosalvipuberulin

Cas No. 115321-32-9 SDF Download SDF
PubChem ID 189288 Appearance Powder
Formula C20H14O5 M.Wt 334.3
Type of Compound Diterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
SMILES CC1=C2C=CCC3=C(C2=CC4=C1C(OC4=O)C5=COC=C5)COC3=O
Standard InChIKey HIBSGIRHUQGFAD-SFHVURJKSA-N
Standard InChI InChI=1S/C20H14O5/c1-10-12-3-2-4-13-16(9-24-19(13)21)14(12)7-15-17(10)18(25-20(15)22)11-5-6-23-8-11/h2-3,5-8,18H,4,9H2,1H3/t18-/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 Isosalvipuberulin

The aerial parts of Salvia dugesii

Biological Activity of Isosalvipuberulin

DescriptionStandard reference

Protocol of Isosalvipuberulin

Structure Identification
Org Lett. 2014 Jun 20;16(12):3376-9.

Diastereoselective total synthesis of salvileucalin C.[Pubmed: 24895836]


METHODS AND RESULTS:
A concise and efficient approach for the diastereoselective total synthesis of salvileucalin C, as well as their biosynthetically related diterpenoids salvileucalin D, salvipuberulin, Isosalvipuberulin, and dugesin B, has been reported for the first time.
CONCLUSIONS:
The key features of the strategy are based on a Beckwith-Dowd ring expansion, a tandem diastereoselective Stille coupling/debromination/desilylation/lactonization reaction, and a photoinduced electrocyclic ring contraction.

Isosalvipuberulin Dilution Calculator

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Isosalvipuberulin Molarity Calculator

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Preparing Stock Solutions of Isosalvipuberulin

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.9913 mL 14.9566 mL 29.9133 mL 59.8265 mL 74.7831 mL
5 mM 0.5983 mL 2.9913 mL 5.9827 mL 11.9653 mL 14.9566 mL
10 mM 0.2991 mL 1.4957 mL 2.9913 mL 5.9827 mL 7.4783 mL
50 mM 0.0598 mL 0.2991 mL 0.5983 mL 1.1965 mL 1.4957 mL
100 mM 0.0299 mL 0.1496 mL 0.2991 mL 0.5983 mL 0.7478 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 Isosalvipuberulin

Diastereoselective total synthesis of salvileucalin C.[Pubmed:24895836]

Org Lett. 2014 Jun 20;16(12):3376-9.

A concise and efficient approach for the diastereoselective total synthesis of salvileucalin C, as well as their biosynthetically related diterpenoids salvileucalin D, salvipuberulin, Isosalvipuberulin, and dugesin B, has been reported for the first time. The key features of the strategy are based on a Beckwith-Dowd ring expansion, a tandem diastereoselective Stille coupling/debromination/desilylation/lactonization reaction, and a photoinduced electrocyclic ring contraction.

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