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H31204

Sigma-Aldrich

9-Hydroxyfluoren

96%

Synonym(e):

9-Fluorenol

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About This Item

Empirische Formel (Hill-System):
C13H10O
CAS-Nummer:
1689-64-1
Molekulargewicht:
182.22
EG-Nummer:
216-879-0
MDL-Nummer:
MFCD00001135
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24895548
NACRES:
NA.22

Assay

96%

mp (Schmelzpunkt)

153-154 °C (lit.)

SMILES String

OC1c2ccccc2-c3ccccc13

InChI

1S/C13H10O/c14-13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)13/h1-8,13-14H

InChIKey

AFMVESZOYKHDBJ-UHFFFAOYSA-N

Verwandte Kategorien

Piktogramme

Environment
GHS09

Signalwort

Warning

H-Sätze

H410

Gefahreneinstufungen

Aquatic Acute 1 - Aquatic Chronic 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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L Bastiaens et al.
Research in microbiology, 152(10), 849-859 (2002-01-05)
The promoter probe mini-Tn5-luxAB-tet was used to create a luxAB transcriptional fusion responding to fluorene in the fluorene utilising bacterium Sphingomonas sp. LB126. The mutant strain, named L-132, was impaired in fluorene utilisation and strongly emitted light upon addition of
C Chen et al.
Drug metabolism and disposition: the biological fate of chemicals, 12(4), 421-426 (1984-07-01)
Fluoren-9-ol and fluoren-9-one were used as model substrates to study microsomal metabolism of alcohols and carbonyl compounds. It was found that there was an oxidoreductase(s) present in the microsomal preparation that catalyzed interconversion of this alcohol and ketone using pyridine
Pooja V Reddy et al.
Archives of microbiology, 200(1), 171-182 (2017-09-25)
A high-efficiency fluoranthene-degrading bacterium Paenibacillus sp. PRNK-6 was isolated from PAH-contaminated soil. The strain degrades 96% (240 mg l
Derek Dunn et al.
Bioorganic & medicinal chemistry letters, 22(11), 3751-3753 (2012-05-02)
In searching for a next generation molecule to the novel wake promoting agent modafinil (compound 1), a series of fluorene-derived wakefulness enhancing agents were developed and evaluated in rat. Extensive pharmacokinetic studies of a potent member of the series (compound
Biban Gill et al.
Analytical and bioanalytical chemistry, 411(7), 1397-1407 (2019-01-27)
Urinary 1-hydroxypyrene (OH-Pyr) is widely used for biomonitoring human exposures to polycyclic aromatic hydrocarbons (PAHs) from air pollution and tobacco smoke. However, there have been few rigorous validation studies reported to ensure reliable OH-Pyr determination for occupational health and risk
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