Acerogenin G

CAS# 130233-83-9

Acerogenin G

Catalog No. BCN7328----Order now to get a substantial discount!

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

Quality Control of Acerogenin G

Number of papers citing our products

Chemical structure

Acerogenin G

3D structure

Chemical Properties of Acerogenin G

Cas No. 130233-83-9 SDF Download SDF
PubChem ID 14608480 Appearance Oil
Formula C19H22O3 M.Wt 298.38
Type of Compound Phenols Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 1,7-bis(4-hydroxyphenyl)heptan-3-one
SMILES C1=CC(=CC=C1CCCCC(=O)CCC2=CC=C(C=C2)O)O
Standard InChIKey QUHYUSAHBDACNG-UHFFFAOYSA-N
Standard InChI InChI=1S/C19H22O3/c20-17(10-7-16-8-13-19(22)14-9-16)4-2-1-3-15-5-11-18(21)12-6-15/h5-6,8-9,11-14,21-22H,1-4,7,10H2
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 Acerogenin G

The stem barks of Acer nikoense

Biological Activity of Acerogenin G

DescriptionAcerogenin G is a natural product from Acer nikoense.

Protocol of Acerogenin G

Structure Identification
Tetrahedron, 2013, 69(13):2807-2815.

Total synthesis of acerogenins E, G and K, and centrolobol.[Reference: WebLink]


METHODS AND RESULTS:
The first total synthesis of the diarylheptanoid acerogenins E and K, isolated from Acer nikoense MAXIM., is described. Formation of the 13-membered m,m-cyclophane skeleton was successfully achieved on the basis of a domino process involving a Miyaura arylborylation–intramolecular Suzuki reaction. The cyclization precursor was prepared via a Wittig reaction and Claisen–Schmidt condensation, which proceeded in moderate yields.
CONCLUSIONS:
The total synthesis of Acerogenin G and centrolobol was also achieved from a common synthetic intermediate.

Acerogenin G Dilution Calculator

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Acerogenin G Molarity Calculator

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Preparing Stock Solutions of Acerogenin G

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.3514 mL 16.7572 mL 33.5143 mL 67.0286 mL 83.7858 mL
5 mM 0.6703 mL 3.3514 mL 6.7029 mL 13.4057 mL 16.7572 mL
10 mM 0.3351 mL 1.6757 mL 3.3514 mL 6.7029 mL 8.3786 mL
50 mM 0.067 mL 0.3351 mL 0.6703 mL 1.3406 mL 1.6757 mL
100 mM 0.0335 mL 0.1676 mL 0.3351 mL 0.6703 mL 0.8379 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 Acerogenin G

Total synthesis of acerogenins E, G and K, and centrolobol.

Tetrahedron, 2013, 69(13):2807-2815.

The first total synthesis of the diarylheptanoid acerogenins E and K, isolated from Acer nikoense MAXIM., is described. Formation of the 13-membered m,m-cyclophane skeleton was successfully achieved on the basis of a domino process involving a Miyaura arylborylation–intramolecular Suzuki reaction. The cyclization precursor was prepared via a Wittig reaction and Claisen–Schmidt condensation, which proceeded in moderate yields. The total synthesis of Acerogenin G and centrolobol was also achieved from a common synthetic intermediate.

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