Paeonilactone A

CAS# 98751-79-2

Paeonilactone A

Catalog No. BCN3967----Order now to get a substantial discount!

Product Name & Size Price Stock
Paeonilactone A: 5mg $886 In Stock
Paeonilactone A: 10mg Please Inquire In Stock
Paeonilactone A: 20mg Please Inquire Please Inquire
Paeonilactone A: 50mg Please Inquire Please Inquire
Paeonilactone A: 100mg Please Inquire Please Inquire
Paeonilactone A: 200mg Please Inquire Please Inquire
Paeonilactone A: 500mg Please Inquire Please Inquire
Paeonilactone A: 1000mg Please Inquire Please Inquire

Quality Control of Paeonilactone A

Number of papers citing our products

Chemical structure

Paeonilactone A

3D structure

Chemical Properties of Paeonilactone A

Cas No. 98751-79-2 SDF Download SDF
PubChem ID 10081437 Appearance Powder
Formula C10H14O4 M.Wt 198.2
Type of Compound Monoterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (3R,3aR,6S,7aR)-6-hydroxy-3,6-dimethyl-3a,4,7,7a-tetrahydro-3H-1-benzofuran-2,5-dione
SMILES CC1C2CC(=O)C(CC2OC1=O)(C)O
Standard InChIKey NODZICYHUGDVAM-IBNKKVAHSA-N
Standard InChI InChI=1S/C10H14O4/c1-5-6-3-8(11)10(2,13)4-7(6)14-9(5)12/h5-7,13H,3-4H2,1-2H3/t5-,6-,7-,10+/m1/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 Paeonilactone A

The roots of Paeonia albiflora

Biological Activity of Paeonilactone A

DescriptionStandard reference

Protocol of Paeonilactone A

Structure Identification
J Org Chem. 2000 Apr 7;65(7):2122-6.

An enantioselective route to paeonilactone A via palladium- and copper-catalyzed reactions.[Pubmed: 10774035]


METHODS AND RESULTS:
We herein report on a formal total synthesis of Paeonilactone A involving palladium-, copper-, and enzyme-catalyzed reactions starting from 1,3-cyclohexadiene. The key step in the synthesis, a palladium(II)-catalyzed 1,4-oxylactonization of a conjugated diene, simultaneously introduces two of the oxygen substituents required for the target molecule. The synthesis also includes our recently developed copper(I)-catalyzed cross-coupling reaction between dienyltriflates with Grignard reagents, introducing one of the methyl groups present in the target molecule.
CONCLUSIONS:
This new approach toward Paeonilactone A allows complete control of all four stereogenic centers and is the first enantioselective route toward Paeonilactone A starting from an achiral substrate.

Fitoterapia. 2007 Jan;78(1):76-8.

Monoterpene glycosides from Paeonia delavayi.[Pubmed: 17067761]


METHODS AND RESULTS:
A new monoterpene glycoside, 4-O-methyl-4''-hydroxy-3''-methoxy-paeoniflorin (1), was isolated from the root cortex of Paeonia delavayi along with the known paeoniflorin, oxypaeoniflorin, benzoylpaeoniflorin, benzoyloxypaeoniflorin, albiflorin and a Paeonilactone A.

Paeonilactone A Dilution Calculator

Concentration (start)
x
Volume (start)
=
Concentration (final)
x
Volume (final)
 
 
 
C1
V1
C2
V2

calculate

Paeonilactone A Molarity Calculator

Mass
=
Concentration
x
Volume
x
MW*
 
 
 
g/mol

calculate

Preparing Stock Solutions of Paeonilactone A

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.0454 mL 25.227 mL 50.4541 mL 100.9082 mL 126.1352 mL
5 mM 1.0091 mL 5.0454 mL 10.0908 mL 20.1816 mL 25.227 mL
10 mM 0.5045 mL 2.5227 mL 5.0454 mL 10.0908 mL 12.6135 mL
50 mM 0.1009 mL 0.5045 mL 1.0091 mL 2.0182 mL 2.5227 mL
100 mM 0.0505 mL 0.2523 mL 0.5045 mL 1.0091 mL 1.2614 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.

Organizitions Citing Our Products recently

 
 
 

Calcutta University

University of Minnesota

University of Maryland School of Medicine

University of Illinois at Chicago

The Ohio State University

University of Zurich

Harvard University

Colorado State University

Auburn University

Yale University

Worcester Polytechnic Institute

Washington State University

Stanford University

University of Leipzig

Universidade da Beira Interior

The Institute of Cancer Research

Heidelberg University

University of Amsterdam

University of Auckland
TsingHua University
TsingHua University
The University of Michigan
The University of Michigan
Miami University
Miami University
DRURY University
DRURY University
Jilin University
Jilin University
Fudan University
Fudan University
Wuhan University
Wuhan University
Sun Yat-sen University
Sun Yat-sen University
Universite de Paris
Universite de Paris
Deemed University
Deemed University
Auckland University
Auckland University
The University of Tokyo
The University of Tokyo
Korea University
Korea University
Featured Products
New Products
 

References on Paeonilactone A

An enantioselective route to paeonilactone A via palladium- and copper-catalyzed reactions.[Pubmed:10774035]

J Org Chem. 2000 Apr 7;65(7):2122-6.

We herein report on a formal total synthesis of Paeonilactone A involving palladium-, copper-, and enzyme-catalyzed reactions starting from 1,3-cyclohexadiene. The key step in the synthesis, a palladium(II)-catalyzed 1,4-oxylactonization of a conjugated diene, simultaneously introduces two of the oxygen substituents required for the target molecule. The synthesis also includes our recently developed copper(I)-catalyzed cross-coupling reaction between dienyltriflates with Grignard reagents, introducing one of the methyl groups present in the target molecule. This new approach toward Paeonilactone A allows complete control of all four stereogenic centers and is the first enantioselective route toward Paeonilactone A starting from an achiral substrate.

Monoterpene glycosides from Paeonia delavayi.[Pubmed:17067761]

Fitoterapia. 2007 Jan;78(1):76-8.

A new monoterpene glycoside, 4-O-methyl-4''-hydroxy-3''-methoxy-paeoniflorin (1), was isolated from the root cortex of Paeonia delavayi along with the known paeoniflorin, oxypaeoniflorin, benzoylpaeoniflorin, benzoyloxypaeoniflorin, albiflorin and a paeonilactone-A.

Keywords:

Paeonilactone A,98751-79-2,Natural Products, buy Paeonilactone A , Paeonilactone A supplier , purchase Paeonilactone A , Paeonilactone A cost , Paeonilactone A manufacturer , order Paeonilactone A , high purity Paeonilactone A

Online Inquiry for:

      Fill out the information below

      • Size:Qty: - +

      * Required Fields

                                      Result: