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Dihydropyrocurzerenone

CAS# 59462-26-9

Dihydropyrocurzerenone

Catalog No. BCN8061----Order now to get a substantial discount!

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Quality Control of Dihydropyrocurzerenone

Number of papers citing our products

Chemical structure

Dihydropyrocurzerenone

3D structure

Chemical Properties of Dihydropyrocurzerenone

Cas No. 59462-26-9 SDF Download SDF
PubChem ID 91734838 Appearance Powder
Formula C15H18O M.Wt 214.30
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (8R)-1,5,8-trimethyl-6,7,8,9-tetrahydrobenzo[e][1]benzofuran
SMILES CC1CCC2=C(C1)C3=C(C=C2C)OC=C3C
Standard InChIKey GWQCNWWIXOLIAV-SECBINFHSA-N
Standard InChI InChI=1S/C15H18O/c1-9-4-5-12-10(2)7-14-15(13(12)6-9)11(3)8-16-14/h7-9H,4-6H2,1-3H3/t9-/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 Dihydropyrocurzerenone

The herbs of Chloranthus sertusra

Protocol of Dihydropyrocurzerenone

Structure Identification
Fitoterapia. 2002 Feb;73(1):48-55.

Furanosesquiterpenes from Commiphora sphaerocarpa and related adulterants of true myrrh.[Pubmed: 11864764]


METHODS AND RESULTS:
A new furanosesquiterpene, (1E)-8,12-epoxygermacra-1,7,10,11-tetraen-6-one (3), was isolated from the resin of Commiphora sphaerocarpa together with the known compounds curzerenone (1), furanodienone (2), (1E)-3-methoxy-8,12-epoxygermacra-1,7,10,11-tetraen-6-one (4), (1(10)E,2R*,4R*)-2-methoxy-8,12-epoxygermacra- 1(10),7,11-trien-6-one (5), and Dihydropyrocurzerenone (6). Hydrodistillates of the resins of C. sphaerocarpa, C. holtziana, C. kataf and C. myrrha were analysed.
CONCLUSIONS:
The identifications were aided by NMR, GC and GC-MS.

Dihydropyrocurzerenone Dilution Calculator

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Dihydropyrocurzerenone Molarity Calculator

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Preparing Stock Solutions of Dihydropyrocurzerenone

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.6664 mL 23.3318 mL 46.6636 mL 93.3271 mL 116.6589 mL
5 mM 0.9333 mL 4.6664 mL 9.3327 mL 18.6654 mL 23.3318 mL
10 mM 0.4666 mL 2.3332 mL 4.6664 mL 9.3327 mL 11.6659 mL
50 mM 0.0933 mL 0.4666 mL 0.9333 mL 1.8665 mL 2.3332 mL
100 mM 0.0467 mL 0.2333 mL 0.4666 mL 0.9333 mL 1.1666 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 Dihydropyrocurzerenone

Furanosesquiterpenes from Commiphora sphaerocarpa and related adulterants of true myrrh.[Pubmed:11864764]

Fitoterapia. 2002 Feb;73(1):48-55.

A new furanosesquiterpene, (1E)-8,12-epoxygermacra-1,7,10,11-tetraen-6-one (3), was isolated from the resin of Commiphora sphaerocarpa together with the known compounds curzerenone (1), furanodienone (2), (1E)-3-methoxy-8,12-epoxygermacra-1,7,10,11-tetraen-6-one (4), (1(10)E,2R*,4R*)-2-methoxy-8,12-epoxygermacra- 1(10),7,11-trien-6-one (5), and Dihydropyrocurzerenone (6). Hydrodistillates of the resins of C. sphaerocarpa, C. holtziana, C. kataf and C. myrrha were analysed. The identifications were aided by NMR, GC and GC-MS.

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