H31204
9-Hydroxyfluoren
96%
Synonym(e):
9-Fluorenol
Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(3)
About This Item
Empirische Formel (Hill-System):
C13H10O
CAS-Nummer:
Molekulargewicht:
182.22
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
Empfohlene Produkte
Qualitätsniveau
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
Signalwort
Warning
H-Sätze
P-Sätze
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)
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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
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
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
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