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4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone

CAS# 263368-91-8

4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone

Catalog No. BCN1469----Order now to get a substantial discount!

Product Name & Size Price Stock
4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone: 5mg $799 In Stock
4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone: 10mg Please Inquire In Stock
4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone: 20mg Please Inquire Please Inquire
4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone: 50mg Please Inquire Please Inquire
4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone: 100mg Please Inquire Please Inquire
4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone: 200mg Please Inquire Please Inquire
4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone: 500mg Please Inquire Please Inquire
4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone: 1000mg Please Inquire Please Inquire
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Quality Control of 4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone

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Chemical structure

4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone

3D structure

Chemical Properties of 4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone

Cas No. 263368-91-8 SDF Download SDF
PubChem ID 10753168 Appearance Powder
Formula C13H14O5 M.Wt 250.25
Type of Compound Phenols Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (3R,4R)-4-acetyl-3,6,8-trihydroxy-3-methyl-2,4-dihydronaphthalen-1-one
SMILES CC(=O)C1C2=CC(=CC(=C2C(=O)CC1(C)O)O)O
Standard InChIKey QDNOAZOXGLUUEB-CHWSQXEVSA-N
Standard InChI InChI=1S/C13H14O5/c1-6(14)12-8-3-7(15)4-9(16)11(8)10(17)5-13(12,2)18/h3-4,12,15-16,18H,5H2,1-2H3/t12-,13-/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 4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone

The herbs of Cassia siamea

Biological Activity of 4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone

Description4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone is a natural product from Caesalpinia minax.

Protocol of 4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone

Structure Identification
Zhongguo Zhong Yao Za Zhi. 2013 Apr;38(7):1014-7.

Phenolic compounds from Caesalpinia minax.[Pubmed: 23847948]


METHODS AND RESULTS:
Fifteen compounds were obtained from the twigs and leaves of Caesalpinia minax. Their structures were identified as apigenin (1), 5,7,3',4'- tetrahydroxy-3-methoxyflavone (2), luteolin-5, 3 '-dimethyl-ether (3), thevetiaflavon (4), apigenin-7-O-beta-D-glucuronide (5), bonducellin (6), 7-hydroxy-3-( 4-hydroxybenzylidene )-chroman-4-one (7), 3-deoxysappanchalcone (8), 5-acetonyl-7-hydroxy-2-methyl chromone (9), 4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone (10), 4-(cis)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone(11), vanillic acid (12), omega-hydroxypropioquaiacone (13), syringaresinol (14) and uracil (15). All compounds were isolated from C. minax for the first time.
CONCLUSIONS:
Compounds 1-14 were phenolic compounds and compounds 1-5, 9-13 and 15 were isolated from the genus Caesalpinia for the first time.

4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone Dilution Calculator

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4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone Molarity Calculator

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Preparing Stock Solutions of 4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.996 mL 19.98 mL 39.96 mL 79.9201 mL 99.9001 mL
5 mM 0.7992 mL 3.996 mL 7.992 mL 15.984 mL 19.98 mL
10 mM 0.3996 mL 1.998 mL 3.996 mL 7.992 mL 9.99 mL
50 mM 0.0799 mL 0.3996 mL 0.7992 mL 1.5984 mL 1.998 mL
100 mM 0.04 mL 0.1998 mL 0.3996 mL 0.7992 mL 0.999 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 4-(trans)-Acetyl-3,6,8-trihydroxy-3-methyldihydronaphthalenone

[Phenolic compounds from Caesalpinia minax].[Pubmed:23847948]

Zhongguo Zhong Yao Za Zhi. 2013 Apr;38(7):1014-7.

Fifteen compounds were obtained from the twigs and leaves of Caesalpinia minax. Their structures were identified as apigenin (1), 5,7,3',4'- tetrahydroxy-3-methoxyflavone (2), luteolin-5, 3 '-dimethyl-ether (3), thevetiaflavon (4), apigenin-7-O-beta-D-glucuronide (5), bonducellin (6), 7-hydroxy-3-( 4-hydroxybenzylidene )-chroman-4-one (7), 3-deoxysappanchalcone (8), 5-acetonyl-7-hydroxy-2-methyl chromone (9), 4-(trans)-acetyl-3,6,8-trihydroxy-3-methyl-dihydronaphthalenone (10), 4-(cis)-acetyl-3,6,8-trihydroxy-3-methyl-dihydronaphthalenone (11), vanillic acid (12), omega-hydroxypropioquaiacone (13), syringaresinol (14) and uracil (15). All compounds were isolated from C. minax for the first time. Compounds 1-14 were phenolic compounds and compounds 1-5, 9-13 and 15 were isolated from the genus Caesalpinia for the first time.

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