Основные атрибуты  химическое свойство Информация о безопасности химические свойства, назначение, производство поставщик Обзор
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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 n20/D 1.504
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 об опасности и безопасности
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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