U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C13H10O
Molecular Weight 182.2179
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 9-HYDROXYFLUORENE

SMILES

OC1C2=CC=CC=C2C3=CC=CC=C13

InChI

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

HIDE SMILES / InChI

Molecular Formula C13H10O
Molecular Weight 182.2179
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
From surface-inspired oxovanadium silsesquioxane models to active catalysts for the oxidation of alcohols with O(2)-the cinnamic acid/metavanadate system.
2010-06-18
Polycyclic aromatic hydrocarbon metabolite levels and pediatric allergy and asthma in an inner-city cohort.
2010-03
Urinary profiles to assess polycyclic aromatic hydrocarbons exposure in coke-oven workers.
2010-01-15
Association of urinary polycyclic aromatic hydrocarbons and serum C-reactive protein.
2010-01
Effect of steric bulk on the absolute reactivity of allene oxides.
2009-11-07
A structure-based investigation on the binding interaction of hydroxylated polycyclic aromatic hydrocarbons with DNA.
2009-08-21
Urinary polycyclic aromatic hydrocarbons and monohydroxy metabolites as biomarkers of exposure in coke oven workers.
2009-08
A novel headspace solid-phase microextraction method using in situ derivatization and a diethoxydiphenylsilane fibre for the gas chromatography-mass spectrometry determination of urinary hydroxy polycyclic aromatic hydrocarbons.
2009-07-24
Involuntary tobacco smoke exposure and urinary levels of polycyclic aromatic hydrocarbons in the United States, 1999 to 2002.
2009-03
Bacterial degradation of aromatic compounds.
2009-01
Characterization of new oxidation products of 9H-carbazole and structure related compounds by biphenyl-utilizing bacteria.
2009-01
Role of surfactants in optimizing fluorene assimilation and intermediate formation by Rhodococcus rhodochrous VKM B-2469.
2009-01
Development of a gas chromatography/mass spectrometry method to quantify several urinary monohydroxy metabolites of polycyclic aromatic hydrocarbons in occupationally exposed subjects.
2008-11-15
Solution structure of a designed spirocyclic helical ligand binding at a two-base bulge site in DNA.
2007-04-24
Oxovanadium(V) tetrathiacalix[4]arene complexes and their activity as oxidation catalysts.
2007
Study of metabolites from the degradation of polycyclic aromatic hydrocarbons (PAHs) by bacterial consortium enriched from mangrove sediments.
2006-12
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Mono- and dinuclear oxovanadium(V)calixarene complexes and their activity as oxidation catalysts.
2006-10-02
Microbial reduction of 9-fluorenone to 9-hydroxyfluorene in carbon-filtered water: a confounding factor in an aquatic bioassay of 9-fluorenone with larvae of the midge, Chironomus tentans (Fabr.).
2005-12
Characterization of [3Fe-4S] ferredoxin DbfA3, which functions in the angular dioxygenase system of Terrabacter sp. strain DBF63.
2005-08
Directed metalation route to ferroelectric liquid crystals with a chiral fluorenol core: the effect of restricted rotation on polar order.
2004-02-04
ap-9-(meta-tert-butylphenyl)fluorene.
2003-10
Toxicity of fluoranthene and its biodegradation metabolites to aquatic organisms.
2003-08
A transcriptional luxAB reporter fusion responding to fluorene in Sphingomonas sp. LB126 and its initial characterisation for whole-cell bioreporter purposes.
2001-12
Solvent-dependent C-OH homolysis and heterolysis in electronically excited 9-fluorenol: the life and solvation time of the 9-fluorenyl cation in water.
2001-04-17
Fluoranthene degradation in Pseudomonas alcaligenes PA-10.
2001
New metabolites in the degradation of fluorene by Arthrobacter sp. strain F101.
1997-03
Regio- and stereospecific oxidation of fluorene, dibenzofuran, and dibenzothiophene by naphthalene dioxygenase from Pseudomonas sp. strain NCIB 9816-4.
1996-11
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 20:48:24 GMT 2025
Edited
by admin
on Mon Mar 31 20:48:24 GMT 2025
Record UNII
BV0Q72R613
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-5320
Preferred Name English
9-HYDROXYFLUORENE
Systematic Name English
FLUOREN-9-OL
Systematic Name English
FLUORENOL
Common Name English
9-FLUORENYL ALCOHOL
Systematic Name English
9-HYDROXY FLUORENE
Systematic Name English
9-FLUORENOL
Systematic Name English
9-HYDROXY-9H-FLUORENE
Systematic Name English
9H-FLUOREN-9-OL
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID4052683
Created by admin on Mon Mar 31 20:48:24 GMT 2025 , Edited by admin on Mon Mar 31 20:48:24 GMT 2025
PRIMARY
NSC
5320
Created by admin on Mon Mar 31 20:48:24 GMT 2025 , Edited by admin on Mon Mar 31 20:48:24 GMT 2025
PRIMARY
FDA UNII
BV0Q72R613
Created by admin on Mon Mar 31 20:48:24 GMT 2025 , Edited by admin on Mon Mar 31 20:48:24 GMT 2025
PRIMARY
WIKIPEDIA
Fluorenol
Created by admin on Mon Mar 31 20:48:24 GMT 2025 , Edited by admin on Mon Mar 31 20:48:24 GMT 2025
PRIMARY
PUBCHEM
74318
Created by admin on Mon Mar 31 20:48:24 GMT 2025 , Edited by admin on Mon Mar 31 20:48:24 GMT 2025
PRIMARY
CHEBI
16904
Created by admin on Mon Mar 31 20:48:24 GMT 2025 , Edited by admin on Mon Mar 31 20:48:24 GMT 2025
PRIMARY
CAS
1689-64-1
Created by admin on Mon Mar 31 20:48:24 GMT 2025 , Edited by admin on Mon Mar 31 20:48:24 GMT 2025
PRIMARY
ECHA (EC/EINECS)
216-879-0
Created by admin on Mon Mar 31 20:48:24 GMT 2025 , Edited by admin on Mon Mar 31 20:48:24 GMT 2025
PRIMARY