Macrocarpal O

CAS# 327622-65-1

Macrocarpal O

2D Structure

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Macrocarpal O: 5mg $1150 In Stock
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Macrocarpal O

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Chemical Properties of Macrocarpal O

Cas No. 327622-65-1 SDF Download SDF
PubChem ID 9956473 Appearance Powder
Formula C28H40O6 M.Wt 472.62
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 5-[(1S)-1-[(1R,3aR,4R,7R)-7-(2-hydroxypropan-2-yl)-1,4-dimethyl-3,3a,4,5,6,7-hexahydro-2H-azulen-1-yl]-3-methylbutyl]-2,4,6-trihydroxybenzene-1,3-dicarbaldehyde
SMILES CC1CCC(C=C2C1CCC2(C)C(CC(C)C)C3=C(C(=C(C(=C3O)C=O)O)C=O)O)C(C)(C)O
Standard InChIKey VUKIJLQDSQXHDI-BBHKXTTBSA-N
Standard InChI InChI=1S/C28H40O6/c1-15(2)11-22(23-25(32)19(13-29)24(31)20(14-30)26(23)33)28(6)10-9-18-16(3)7-8-17(12-21(18)28)27(4,5)34/h12-18,22,31-34H,7-11H2,1-6H3/t16-,17-,18-,22-,28+/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 Macrocarpal O

The leaves of Eucalyptus globulus.

Biological Activity of Macrocarpal O

DescriptionMacrocarpal O is a natural product from Eucalyptus globulus.

Protocol of Macrocarpal O

Structure Identification
Phytochemistry Letters, 2015, 11:69-73.

New formylated phloroglucinol compounds from Eucalyptus globulus foliage.[Reference: WebLink]


METHODS AND RESULTS:
Eucalyptus globulus Labill and identified as macrocarpal P (1) and macrocarpal Q (2). Structural elucidations were carried out using conventional 1D and 2D NMR and mass spectrometry together with complementary techniques (UV and IR).
CONCLUSIONS:
Macrocarpal Q was a diastereoisomer of macrocarpal E (3), configuration of which was not precised. Simultaneous isolation of macrocarpals E and Q allowed to determine the configurations of both compounds. The diformylphloroglucinol (4) was also isolated as well as already known compounds grandinol, macrocarpals D, macrocarpal I, macrocarpal L, macrocarpal N, Macrocarpal O and macrocarpal am-1.

Macrocarpal O Dilution Calculator

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Macrocarpal O Molarity Calculator

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Preparing Stock Solutions of Macrocarpal O

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.1159 mL 10.5793 mL 21.1586 mL 42.3173 mL 52.8966 mL
5 mM 0.4232 mL 2.1159 mL 4.2317 mL 8.4635 mL 10.5793 mL
10 mM 0.2116 mL 1.0579 mL 2.1159 mL 4.2317 mL 5.2897 mL
50 mM 0.0423 mL 0.2116 mL 0.4232 mL 0.8463 mL 1.0579 mL
100 mM 0.0212 mL 0.1058 mL 0.2116 mL 0.4232 mL 0.529 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 Macrocarpal O

New formylated phloroglucinol compounds from Eucalyptus globulus foliage.

Phytochemistry Letters, 2015, 11:69-73.

Eucalyptus globulus Labill and identified as macrocarpal P (1) and macrocarpal Q (2). Structural elucidations were carried out using conventional 1D and 2D NMR and mass spectrometry together with complementary techniques (UV and IR). Macrocarpal Q was a diastereoisomer of macrocarpal E (3), configuration of which was not precised. Simultaneous isolation of macrocarpals E and Q allowed to determine the configurations of both compounds. The diformylphloroglucinol (4) was also isolated as well as already known compounds grandinol, macrocarpals D, macrocarpal I, macrocarpal L, macrocarpal N, Macrocarpal O and macrocarpal am-1.

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