Home Aldehydes 1-Hydroxy-2-naphthaldehyde

1-Hydroxy-2-naphthaldehyde

CAS No.:
574-96-9
Catalog Number:
AG0032S9
Molecular Formula:
C11H8O2
Molecular Weight:
172.1800
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$57
- +
5g
98%
In Stock USA
United States
$238
- +
25g
98%
In Stock USA
United States
$950
- +
Product Description
Catalog Number:
AG0032S9
Chemical Name:
1-Hydroxy-2-naphthaldehyde
CAS Number:
574-96-9
Molecular Formula:
C11H8O2
Molecular Weight:
172.1800
MDL Number:
MFCD00092325
IUPAC Name:
1-hydroxynaphthalene-2-carbaldehyde
InChI:
InChI=1S/C11H8O2/c12-7-9-6-5-8-3-1-2-4-10(8)11(9)13/h1-7,13H
InChI Key:
OITQDWKMIPXGFL-UHFFFAOYSA-N
SMILES:
O=Cc1ccc2c(c1O)cccc2
Properties
Complexity:
191  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
172.052g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
172.183g/mol
Monoisotopic Mass:
172.052g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
37.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.6  
Literature
Title Journal
The phn Island: A New Genomic Island Encoding Catabolism of Polynuclear Aromatic Hydrocarbons. Frontiers in microbiology 20120101
Tautomerism in Schiff bases. The cases of 2-hydroxy-1-naphthaldehyde and 1-hydroxy-2-naphthaldehyde investigated in solution and the solid state. Organic & biomolecular chemistry 20111221
Fluorescence excitation and excited state intramolecular proton transfer of jet-cooled naphthol derivatives: part 2. 2-Hydroxy-1-naphthaldehyde. Physical chemistry chemical physics : PCCP 20111107
Fluorescence excitation and excited state intramolecular proton transfer of jet-cooled naphthol derivatives: Part 1. 1-Hydroxy-2-naphthaldehyde. Physical chemistry chemical physics : PCCP 20110428
Inequivalence of substitution pairs in hydroxynaphthaldehyde: A theoretical measurement by intramolecular hydrogen bond strength, aromaticity, and excited-state intramolecular proton transfer reaction. Journal of computational chemistry 20110115
Coordination in phenanthrene biodegradation: pyruvate as microbial demarcation. Bulletin of environmental contamination and toxicology 20101201
Modulated photophysics of an ESIPT probe 1-hydroxy-2-naphthaldehyde within motionally restricted environments of liposome membranes having varying surface charges. The journal of physical chemistry. B 20101007
{3-Methyl-2-[(1-oxido-2-naphth-yl)methyl-idene-amino-κO,N]butano-ato-κO}(1H-pyrazole-κN)nickel(II). Acta crystallographica. Section E, Structure reports online 20100901
4-[(1-Hy-droxy-2-naphth-yl)methyl-ene-amino]-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one. Acta crystallographica. Section E, Structure reports online 20100801
Modulation of excited-state intramolecular proton transfer reaction of 1-hydroxy-2-naphthaldehyde in different supramolecular assemblies. Langmuir : the ACS journal of surfaces and colloids 20100302
[Phenanthrene and anthracene degradation by microorganisms of the genus Rhodococcus]. Prikladnaia biokhimiia i mikrobiologiia 20090101
Bacterial degradation of aromatic compounds. International journal of environmental research and public health 20090101
Study of interaction of proton transfer probe 1-hydroxy-2-naphthaldehyde with serum albumins: a spectroscopic study. Journal of photochemistry and photobiology. B, Biology 20080425
Synthesis of water-soluble phenylazosalicylaldehyde analogues and their application to capillary electrophoretic determination of primary amines. Electrophoresis 20060901
Cloning and characterization of a chromosomal gene cluster, pah, that encodes the upper pathway for phenanthrene and naphthalene utilization by Pseudomonas putida OUS82. Journal of bacteriology 19940401
OXIDATIVE METABOLISM OF PHENANTHRENE AND ANTHRACENE BY SOIL PSEUDOMONADS. THE RING-FISSION MECHANISM. The Biochemical journal 19650601
Properties