9-히드록시플루오렌

9-히드록시플루오렌
9-히드록시플루오렌 구조식 이미지
카스 번호:
1689-64-1
한글명:
9-히드록시플루오렌
동의어(한글):
9-하이드록시플루오렌;9-히드록시플루오렌;9-플루오레놀
상품명:
9-Fluorenol
동의어(영문):
hydrafinil;9h-fluoren-9-ol;9-HYDROXYFLUORENE;uorenoL;Hydranafil;1689-64- 1;9-FLUORENOL;fluoren-9-ol;Hydroxyfluoren;9-Fluorenol>
CBNumber:
CB5476145
분자식:
C13H10O
포뮬러 무게:
182.22
MOL 파일:
1689-64-1.mol
MSDS 파일:
SDS

9-히드록시플루오렌 속성

녹는점
153-154 °C(lit.)
끓는 점
275.62°C (rough estimate)
밀도
1.0368 (rough estimate)
굴절률
1.5994 (estimate)
저장 조건
Sealed in dry,Room Temperature
용해도
클로로포름(약간 용해됨), 메탄올(약간 용해됨)
물리적 상태
결정성 분말
산도 계수 (pKa)
13.34±0.20(Predicted)
색상
크림색
수용성
물에 불용성.
BRN
1869799
안정성
안정적인. 타기 쉬운. 강한 산화제와 호환되지 않습니다.
CAS 데이터베이스
1689-64-1(CAS DataBase Reference)
NIST
9H-fluoren-9-ol(1689-64-1)
EPA
9-Hydroxyfluorene (1689-64-1)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi
위험 카페고리 넘버 36/37/38
안전지침서 24/25-36/37/39-27-26
유엔번호(UN No.) UN 3077 9/PG III
WGK 독일 3
위험 참고 사항 Irritant
TSCA Yes
위험 등급 9
포장분류 III
HS 번호 29062990
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H411 장기적 영향에 의해 수생생물에 유독함 수생 환경유해성 물질 - 만성 구분 2
예방조치문구:
P273 환경으로 배출하지 마시오.
P391 누출물을 모으시오.
NFPA 704
0
1 0

9-히드록시플루오렌 C화학적 특성, 용도, 생산

화학적 성질

white powder

용도

9-Fluorenol is used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuffs.

정의

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.

주요 응용

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.

제조 방법

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

Synthesis

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.
synthetic method of 9-FluorenolFig the synthetic method of 9-Fluorenol

9-히드록시플루오렌 준비 용품 및 원자재

원자재

준비 용품


9-히드록시플루오렌 공급 업체

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Capot Chemical Co.,Ltd.
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