Home Aldehydes 574-96-9
574-96-9,MFCD00092325
Catalog No.:AA0032PH

574-96-9 | 1-Hydroxy-2-naphthaldehyde

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250mg
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$25.00   $18.00
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1g
98%
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$58.00   $41.00
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5g
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$273.00   $192.00
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25g
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  • Technical Information
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  • Literature
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  • Technical Information
  • Properties
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Technical Information
Catalog Number:
AA0032PH
Chemical Name:
1-Hydroxy-2-naphthaldehyde
CAS Number:
574-96-9
Molecular Formula:
C11H8O2
Molecular Weight:
172.1800
MDL Number:
MFCD00092325
SMILES:
O=Cc1ccc2c(c1O)cccc2
Properties
Properties
 
BP:
317°C at 760 mmHg  
Form:
Solid  
MP:
56°C  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
191  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
2.6  

Literature

Title: The phn Island: A New Genomic Island Encoding Catabolism of Polynuclear Aromatic Hydrocarbons.

Journal: Frontiers in microbiology 20120101

Title: Tautomerism in Schiff bases. The cases of 2-hydroxy-1-naphthaldehyde and 1-hydroxy-2-naphthaldehyde investigated in solution and the solid state.

Journal: Organic & biomolecular chemistry 20111221

Title: Fluorescence excitation and excited state intramolecular proton transfer of jet-cooled naphthol derivatives: part 2. 2-Hydroxy-1-naphthaldehyde.

Journal: Physical chemistry chemical physics : PCCP 20111107

Title: Fluorescence excitation and excited state intramolecular proton transfer of jet-cooled naphthol derivatives: Part 1. 1-Hydroxy-2-naphthaldehyde.

Journal: Physical chemistry chemical physics : PCCP 20110428

Title: Inequivalence of substitution pairs in hydroxynaphthaldehyde: A theoretical measurement by intramolecular hydrogen bond strength, aromaticity, and excited-state intramolecular proton transfer reaction.

Journal: Journal of computational chemistry 20110115

Title: Coordination in phenanthrene biodegradation: pyruvate as microbial demarcation.

Journal: Bulletin of environmental contamination and toxicology 20101201

Title: Modulated photophysics of an ESIPT probe 1-hydroxy-2-naphthaldehyde within motionally restricted environments of liposome membranes having varying surface charges.

Journal: The journal of physical chemistry. B 20101007

Title: {3-Methyl-2-[(1-oxido-2-naphth-yl)methyl-idene-amino-κO,N]butano-ato-κO}(1H-pyrazole-κN)nickel(II).

Journal: Acta crystallographica. Section E, Structure reports online 20100901

Title: 4-[(1-Hy-droxy-2-naphth-yl)methyl-ene-amino]-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one.

Journal: Acta crystallographica. Section E, Structure reports online 20100801

Title: Modulation of excited-state intramolecular proton transfer reaction of 1-hydroxy-2-naphthaldehyde in different supramolecular assemblies.

Journal: Langmuir : the ACS journal of surfaces and colloids 20100302

Title: [Phenanthrene and anthracene degradation by microorganisms of the genus Rhodococcus].

Journal: Prikladnaia biokhimiia i mikrobiologiia 20090101

Title: Bacterial degradation of aromatic compounds.

Journal: International journal of environmental research and public health 20090101

Title: Study of interaction of proton transfer probe 1-hydroxy-2-naphthaldehyde with serum albumins: a spectroscopic study.

Journal: Journal of photochemistry and photobiology. B, Biology 20080425

Title: Synthesis of water-soluble phenylazosalicylaldehyde analogues and their application to capillary electrophoretic determination of primary amines.

Journal: Electrophoresis 20060901

Title: Cloning and characterization of a chromosomal gene cluster, pah, that encodes the upper pathway for phenanthrene and naphthalene utilization by Pseudomonas putida OUS82.

Journal: Journal of bacteriology 19940401

Title: OXIDATIVE METABOLISM OF PHENANTHRENE AND ANTHRACENE BY SOIL PSEUDOMONADS. THE RING-FISSION MECHANISM.

Journal: The Biochemical journal 19650601

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