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CAS RN: 7562-61-0 | 产品编码: U0023
(+)-Usnic Acid
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| 产品编码 | U0023 |
| 纯度/分析方法 | >98.0%(T)(HPLC) |
| 分子式/分子量 | C__1__8H__1__6O__7 = 344.32 |
| 外观与形状（20°C） | 固体 |
| 储存温度 | 室温 (15°C以下阴凉干燥处) |
| 包装和容器 | 1G-Glass Bottle with Plastic Insert （查看图片） |
| CAS RN | 7562-61-0 |
| Reaxys-RN | 96698 |
| PubChem物质ID | 87577753 |
| SDBS (AIST Spectral DB) | 7871 |
| Merck Index (14) | 9893 |
| MDL编号 | MFCD00016878 |
技术规格
| Appearance | Light orange to Yellow to Green powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Purity(Neutralization titration) | min. 98.0 % |
| Melting point | 195.0 to 203.0 °C |
| Specific rotation [a]20/D | +485 to +505 deg(C=0.7, CHCl3) |
| Solubility in Chloroform | almost transparency |
| NMR | confirm to structure |
物性（参考值）
| 熔点 | 200 °C |
| 比旋光度 [α]D | 495° (C=0.7,CHCl3) |
GHS
| 象形图 |
|
| 信号词 | Danger |
| 危险性说明 | H302 : Harmful if swallowed. H370 : Causes damage to organs. |
| 防范说明 | P501 : Dispose of contents/ container to an approved waste disposal plant. P260 : Do not breathe dust/ fume/ gas/ mist/ vapors/ spray. P270 : Do not eat, drink or smoke when using this product. P264 : Wash skin thoroughly after handling. P308 + P311 : IF exposed or concerned: Call a POISON CENTER/doctor. P301 + P312 + P330 : IF SWALLOWED: Call a POISON CENTER/doctor if you feel unwell. Rinse mouth. P405 : Store locked up. |
相关法规
| RTECS# | HP5295050 |
运输信息
| HS编码* | 2932.99-000 |
应用
(+)-Usnic acid: A Lichen Metabolite with Antibiotic and Several Interesting Properties
(+)-Usnic acid is one of the most common and abundant lichen metabolites, and well known its antibiotic and several interesting properties.1,2) It is reported that the (+)-usnic acid is effective against a large variety Gram-positive bacterial stains including multi-resistant stains of Streptococcus aureus, enterococci and mycobacteria. (+)-Usnic acid also appears to be against Streptococcus mutans.
On the chemical structure, the absolute configuration of (+)-usnic acid at 9b position has determined by X-ray analysis to be R. 2,3,4) Of plausible tautomers, the low energy 1-oxo, 3-hydroxy confirmation is preferred according to calculations.1,2,3) The enolic 3-hydroxy group has the strongest acidic character (pKa 4.4) due to an inductive effect of the keto group.2) Recently, (+)-usnic acid derivatives are used as an organic ligand.5)
On the chemical structure, the absolute configuration of (+)-usnic acid at 9b position has determined by X-ray analysis to be R. 2,3,4) Of plausible tautomers, the low energy 1-oxo, 3-hydroxy confirmation is preferred according to calculations.1,2,3) The enolic 3-hydroxy group has the strongest acidic character (pKa 4.4) due to an inductive effect of the keto group.2) Recently, (+)-usnic acid derivatives are used as an organic ligand.5)
References
- Study of the cytotoxic and antimicrobial activities of usnic acid and derivatives
- E. R. Correche, M. Carrasco, M. E. Escudero, L. Velazquez, A. M. S. De Guzman, F. Giannini, R. D. Enriz, E. A. Jauregui, J. P. Cenal, O. S. Giordano, Fitoterapia 1998, 69, 493.
- Molecules of Interest usnic acid (a review)
- New Results on the Chemistry of Lichen Substances, 4.5.13. Usnic Acid and Related Compounds
- The absolute configurations of (+)-usnic and (+)-isousnic acid. X-ray analyses of the (－)-α-phenylethylamine derivative of (+)-usnic acid and of (－)-pseudoplacodiolic acid, a new dibenzofuran, from the lichen Rhizoplaca chrysoleuca.
- Novel chiral molecular tweezer from (+)-usnic acid
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