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(+)-Ledene
- русский язык имя
- английское имя(+)-Ledene
- CAS №21747-46-6
- CBNumberCB7153554
- ФормулаC15H24
- мольный вес204.35
- EINECS244-565-3
- номер MDLMFCD00042613
- файл Mol21747-46-6.mol
химическое свойство
Температура плавления | 269°C |
Температура кипения | 268-270 °C (lit.) |
плотность | 0.927 g/mL at 20 °C (lit.) |
показатель преломления | n |
температура хранения | Refrigerator |
растворимость | Chloroform (Sparingly), Ethanol (Slightly) |
форма | Oil |
цвет | Colourless |
оптическая активность | [α]20/D +68±2°, c = 10% in ethanol |
БРН | 2554786 |
LogP | 6.447 (est) |
FDA UNII | 236ZZ41F70 |
UNSPSC Code | 12352002 |
NACRES | NA.22 |
Заявления о безопасности | 23-24/25 |
WGK Германия | 3 |
(+)-Ledene химические свойства, назначение, производство
Описание
(+)-Ledene, also called leden or viridiflorene, is an organic compound that belongs to the group of 5, 10-cycloaromadendrane sesquiterpenoids. These compounds are derived from the aromadendrane skeleton through a cyclization reaction between carbon atoms 5 and 10. (+)-Ledene is mainly found in saliva and is considered to have low solubility in water and a relatively neutral nature. In cellular environments, (+)-ledene is predominantly present in the cell membrane (predicted based on logP) and cytoplasm.Использование
(+)-Ledene is an essential oil that is synthesized by viridiflorene synthase. It has been studied as an antioxidant, antimicrobial, antibiofilm and to treat various cancers.Определение
ChEBI: Viridiflorene is a carbotricyclic sesquiterpene obtained from several natural sources, including Australian Tea Tree oil (Melaleuca alternifolia.) It is a sesquiterpene and a carbotricyclic compound.Общее описание
(+)-Ledene is a naturally occurring sesquiterpene that can be prepared from (+)-aromadendrene via isomerization.использованная литература
[1] DUC N. TRAN Prof.??Dr. N C. Biomimetic Synthesis of (+)-Ledene, (+)-Viridiflorol, (?)-Palustrol, (+)-Spathulenol, and Psiguadial A, C, and D via the Platform Terpene (+)-Bicyclogermacrene[J]. Chemistry - A European Journal, 2014. DOI:10.1002/chem.201403082.[2] S. L. GWALTNEY K. J S S T Sakata. Bridged to Fused Ring Interchange. Methodology for the Construction of Fused Cycloheptanes and Cyclooctanes. Total Syntheses of Ledol, Ledene, and Compressanolide[J]. The Journal of Organic Chemistry, 1996. DOI:10.1021/jo961005a.
(+)-Ledene поставщик
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