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6-Hydroxyquinoline - 98%, high purity , CAS No.580-16-5
Basic Description
Synonyms
AC-907/25014237 | InChI=1/C9H7NO/c11-8-3-4-9-7(6-8)2-1-5-10-9/h1-6,11H | 1H-1,6-Epoxyquinoline | OVYWMEWYEJLIER-UHFFFAOYSA- | 6-Quinolinoloxine | BRN 0113196 | 6-Chinolinol | CCRIS 4331 | CCRIS-4331 | 2,6-Dihydroxyquinoline;6-Hydroxy-2(1h)-quinolinone | E
Specifications & Purity
≥98%
Storage Temp
Argon charged
Shipped In
Normal
Product Description
6-Hydroxyquinoline is an ideal photoacid system for exploring excited-state proton transfer (ESPT) reactions. The excited-state proton transfer and geminate recombination of 6-hydroxyquinoline encaged in catalytic Na+-exchanged faujasite zeolites X and Y have been explored by measuring steady-state and picosecond time-resolved spectra. 6-Hydroxyquinoline was used in synthesis of 2,6-substituted-benzo[d]thiazole analogs and 2,4-substituted-benzo[d]thiazole analogs.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Quinolines and derivatives
Subclass
Hydroxyquinolines
Intermediate Tree Nodes
Not available
Direct Parent
Hydroxyquinolines
Alternative Parents
1-hydroxy-2-unsubstituted benzenoids Pyridines and derivatives Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Hydroxyquinoline - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Pyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as hydroxyquinolines. These are compounds containing a quinoline moiety bearing a hydroxyl group.
External Descriptors
monohydroxyquinoline
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
Pubchem Sid
488181320
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488181320
IUPAC Name
quinolin-6-ol
INCHI
InChI=1S/C9H7NO/c11-8-3-4-9-7(6-8)2-1-5-10-9/h1-6,11H
InChIKey
OVYWMEWYEJLIER-UHFFFAOYSA-N
Smiles
C1=CC2=C(C=CC(=C2)O)N=C1
Isomeric SMILES
C1=CC2=C(C=CC(=C2)O)N=C1
WGK Germany
3
RTECS
VC4130000
Molecular Weight
145.16
Beilstein
113196
Reaxy-Rn
113196
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=113196&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
air sensitive ;light sensitive
Melt Point(°C)
188-190°C
Molecular Weight
145.160 g/mol
XLogP3
1.800
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
0
Exact Mass
145.053 Da
Monoisotopic Mass
145.053 Da
Topological Polar Surface Area
33.100 Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
138.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
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