| Identification | Back Directory | [Name]
artemisic acid | [CAS]
80286-58-4 | [Synonyms]
Qinghao acid
Qing Hau acid
Artemisia Acid
artemisic acid
Artimisinic Acid
ARTEMISININIC ACID
(+)-artemisinicaci
4,11(13)-Cadinadien-12-oic acid
4,11(13)-AMorphadien-12-oic acid
Dihydroartemisinic Artemisic Acid
2-[[(1R)-4β,7-Dimethyl-1,2,3,4,4aβ,5,6,8aβ-octahydronaphthalen]-1α-yl]acrylic acid
2-((1R,4R,4aS,8aR)-4,7-Dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalen-1-yl)acrylic acid
2-[(1R,4R,4aS,8aR)-4,7-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalen-1-yl]prop-2-enoic acid
1-Naphthaleneaceticacid, 1,2,3,4,4a,5,6,8a-octahydro-4,7-dimethyl-a-methylene-, (1R,4R,4aS,8aR)-
1-Naphthaleneacetic acid, 1,2,3,4,4a,5,6,8a-octahydro-4,7-dimethyl-α-methylene-, (1R,4R,4aS,8aR)- | [Molecular Formula]
C15H22O2 | [MDL Number]
MFCD00238540 | [MOL File]
80286-58-4.mol | [Molecular Weight]
234.337 |
| Chemical Properties | Back Directory | [Melting point ]
129-131℃ | [Boiling point ]
373.6±11.0 °C(Predicted) | [density ]
1.019 | [storage temp. ]
-20°C Freezer, Under inert atmosphere | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
4.32±0.11(Predicted) | [color ]
White to Pale Yellow | [InChI]
InChI=1/C15H22O2/c1-9-4-6-12-10(2)5-7-13(14(12)8-9)11(3)15(16)17/h8,10,12-14H,3-7H2,1-2H3,(H,16,17)/t10-,12+,13+,14+/s3 | [InChIKey]
PLQMEXSCSAIXGB-OGGOGTMWNA-N | [SMILES]
[C@]12([H])C=C(CC[C@@]1([H])[C@@H](CC[C@H]2C(=C)C(=O)O)C)C |&1:0,6,8,11,r| | [LogP]
5.086 (est) |
| Hazard Information | Back Directory | [Uses]
Artemisic Acid is a derivative of Artemisinin (A777500), an antimalarial constituent of the tradional Chinese medicinal herb Artemisia annua L., Compositae, which has been known for almost 2000 years as Qinghao. Antimalarial. | [Definition]
ChEBI: A monocarboxylic acid that is prop-2-enoic acid which is substituted at position 2 by a 4,7-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalen-1-yl group (the 1S,4R,4aS,8aR diastereoisomer). I
is a sesquiterpenoid precursor of artemisinin, obtained from sweet wormwood, Artemisia annua. | [Synthesis]
Jones reagent (1.4 M CrO3 in 2.2 M H2SO4 aqueous solution) was added dropwise to a 1 mL acetone solution containing 0.2 mmol of compound 6 (CAS: 125184-95-4) at 0 °C. The reaction mixture was slowly warmed to room temperature and stirred continuously until complete consumption of Feedstock 6 was confirmed by thin layer chromatography (TLC) monitoring. Upon completion of the reaction, water and dichloromethane (CH2Cl2) were added to the mixture for extraction. The organic layer was separated and washed with distilled water and subsequently dried with anhydrous magnesium sulfate (MgSO4). The solvent was evaporated under reduced pressure to afford the target product 2-((1R,4R,4aS,8aR)-4,7-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalen-1-yl)acrylic acid in quantitative yield (confirmed by LC/MS). Compound 2 can be further converted to DHAA (3) according to Roth and Acton in Journal of the Chemical Society, Chemical Communications (1989, 24, 1998) or by catalytic hydrogenation (see Example 4). | [References]
[1] Patent: US2006/270863, 2006, A1. Location in patent: Page/Page column 19 |
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