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9-Fluorenol
- английское имя9-Fluorenol
- CAS №1689-64-1
- CBNumberCB5476145
- ФормулаC13H10O
- мольный вес182.22
- EINECS216-879-0
- номер MDLMFCD00001135
- файл Mol1689-64-1.mol
химическое свойство
Температура плавления | 153-154 °C(lit.) |
Температура кипения | 275.62°C (rough estimate) |
плотность | 1.0368 (rough estimate) |
показатель преломления | 1.5994 (estimate) |
температура хранения | Sealed in dry,Room Temperature |
растворимость | Chloroform (Slightly), Methanol (Slightly) |
форма | Crystalline Powder |
пка | 13.34±0.20(Predicted) |
цвет | Cream |
Растворимость в воде | Insoluble in water. |
БРН | 1869799 |
Стабильность | Stable. Combustible. Incompatible with strong oxidizing agents. |
Справочник по базе данных CAS | 1689-64-1(CAS DataBase Reference) |
FDA UNII | BV0Q72R613 |
Справочник по химии NIST | 9H-fluoren-9-ol(1689-64-1) |
Система регистрации веществ EPA | 9-Hydroxyfluorene (1689-64-1) |
UNSPSC Code | 12352100 |
NACRES | NA.22 |
Коды опасности | Xi | |||||||||
Заявления о рисках | 36/37/38 | |||||||||
Заявления о безопасности | 24/25-36/37/39-27-26 | |||||||||
РИДАДР | UN 3077 9/PG III | |||||||||
WGK Германия | 3 | |||||||||
Примечание об опасности | Irritant | |||||||||
TSCA | Yes | |||||||||
Класс опасности | 9 | |||||||||
Группа упаковки | III | |||||||||
кода HS | 29062990 | |||||||||
NFPA 704: |
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рисовальное письмо(GHS)
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рисовальное письмо(GHS)
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сигнальный язык
предупреждение
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вредная бумага
H411:Токсично для водных организмов с долгосрочными последствиями.
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оператор предупредительных мер
P273:Избегать попадания в окружающую среду.
P391:Ликвидировать просыпания/проливы/утечки.
P501:Удалить содержимое/ контейнер на утвержденных станциях утилизации отходов.
9-Fluorenol химические свойства, назначение, производство
Химические свойства
white powderИспользование
9-Fluorenol is used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuffs.Определение
ChEBI: 9-Fluorenol is a member of the class of hydroxyfluorenes that is 9H-fluorene substituted by a hydroxy group at position 9 (the non-aromatic carbon). It has a role as an animal metabolite. It is a member of hydroxyfluorenes and a secondary alcohol.прикладной
9-Fluorenol is a wake-promoting agent and is considered a next-generation anti-drowsiness drug. It is also a potential environmental carcinogen.9-Fluorenol is a dopamine reuptake inhibitor with IC50 of 9 μM, and a major metabolite of a compound developed as a wakefulness-promoting agent.
Подготовка
Synthesis of 9-Fluorenol: A 5-g sample of 9-fluorenone is dissolved in 30 mL of warm ethanol in a 100-mL beaker. To this solution is added, dropwise, 10 mL of a reducing reagent, freshly prepared, which consists of 200 mg sodium methoxide,10 mL methanol, and 0.4 g sodium borohydride.This solution is allowed to stand undisturbed for 10-20 min. A color change is observed as the reaction proceeds from the yellow 9-fluorenone to the white 9-fluorenol.The product is precipitated by the addition of 50 mL of water and neutralized with 0.1 M HCl, vacuum filtered, and washed with cold water to remove any residual inorganic salt formed by the excess of the sodium borohydride reagent and hydrochloric acid.The dried crude product is sufficiently pure for characterization by melting point, infrared spectra,and NMR.The crude product melting point is 153°C, with a product yield of 95-100%.A Synthesis of 9-Fluorenol: Sodium Borohydride Reduction of 9-Fluorenone
Синтез
9-Fluorenol is prepared by reacting 9-fluorenone with THF solution of phosphazene under the action of boron catalyst.Add 9-fluorenone (0.8 mmol), a 0.2 M THF solution of phosphazene (80 μL, 0.016 mmol) and a 0.0762 M THF solution of boron catalyst (420 μL, 0.032 mmol) to a scintillation vial with magnetic stir bar in a glove box. Place the scintillation vial in a Parr reactor. Seal the reactor. Pressurize the reactor with hydrogen gas. Heat reaction mixture at 75°C (inside the reactor). Stir the reaction mixture (1000 rpm) for 20 hours at 75°C. Cool the mixture to room temperature and vent the Parr reactor to obtain 9-hydroxyfluoren. Analyze the reaction mixture by 1H NMR spectroscopy using CDCl3 as solvent.
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