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Details

Stereochemistry ACHIRAL
Molecular Formula C10H10N2
Molecular Weight 158.1998
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,8-NAPHTHALENEDIAMINE

SMILES

NC1=CC=CC2=CC=CC(N)=C12

InChI

InChIKey=YFOOEYJGMMJJLS-UHFFFAOYSA-N
InChI=1S/C10H10N2/c11-8-5-1-3-7-4-2-6-9(12)10(7)8/h1-6H,11-12H2

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Template synthesis, spectroscopic, antibacterial, and antifungal studies of trivalent transition metal ion macrocyclic complexes.
2010-08
Structural, electrochemical, phosphate-hydrolysis, DNA binding and cleavage studies of new macrocyclic binuclear nickel(II) complexes.
2010-04-28
Chiral boronate derivatives via catalytic enantioselective conjugate addition of Grignard reagents on 3-boronyl unsaturated esters and thioesters.
2010-04-28
A new highly selective, ratiometric and colorimetric fluorescence sensor for Cu(2+) with a remarkable red shift in absorption and emission spectra based on internal charge transfer.
2010-02-19
Antibacterial and antifungal studies of macrocyclic complexes of trivalent transition metal ions with their spectroscopic approach.
2010-02
N,N'-Dineopentyl-naphthalene-1,8-diamine.
2009-12-04
Antimicrobial active macrocyclic complexes of Cr(III), Mn(III) and Fe(III) with their spectroscopic approach.
2009-08
Biologically active macrocyclic complexes derived from diaminonaphthalene and glyoxal: Template synthesis and spectroscopic approach.
2009-06
Template synthesis and physico-chemical characterization of 14-membered tetraimine macrocyclic complexes, [MLX(2)] [M=Co(II), Ni(II), Cu(II) and Zn(II)]. DNA binding study on [CoLCl(2)] complex.
2009-04
Structural, magnetic, electrochemical, catalytic, DNA binding and cleavage studies of new macrocyclic binuclear copper(II) complexes.
2009-03
Synthesis and spectroscopic studies on complexes of N,N'-bis-(2-pyridinecarboxaldimine)-1,8-diaminonaphthalene (L); DNA binding studies on Cu(II) complex.
2009-01
Hydrogen-bonding one-dimensional chains containing the R4(2)(8) motif in the ammonium salts 1-naphthylammonium iodide and naphthalene-1,8-diyldiammonium diiodide.
2008-09
Efficient solvent-free syntheses of [2]- and [4]rotaxanes.
2008
Group 4 catalysts for ethene polymerization containing tetradentate salicylaldiminato ligands.
2006-12-14
Chimeric antibody-binding Vitreoscilla hemoglobin (VHb) mediates redox-catalysis reaction: new insight into the functional role of VHb.
2006-08-22
Ground and excited states proton transfer reactions of 1,8-diaminonaphthalene in perchloric acid solutions.
2005-09
Visible colorimetric fluoride ion sensors.
2005-06-23
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005-06
Novel photochromic spiroheterocyclic molecules via oxidation of 1,8-diaminonaphthalene.
2005-04-14
A picosecond time-resolved study on prototropic reactions of electronically excited 1,5- and 1,8-diaminonaphthalenes in aqueous solution.
2005-03
Insignificance of P-H...P hydrogen bonding: structural chemistry of neutral and protonated 1,8-di(phosphinyl)naphthalene.
2004-12-08
Unexpected reaction pathways in the reaction of alkoxyalkynylchromium(0) carbenes with aromatic dinucleophiles.
2003-10-17
Waste-free and facile solid-state protection of diamines, anthranilic acid, diols, and polyols with phenylboronic acid.
2003-09-05
A PVC-based 1,8-diaminonaphthalen electrode for selective determination of vanadyl ion.
2003-07-04
Tetraaminoperylenes: their efficient synthesis and physical properties.
2002-08-16
Synthesis of mono- and difluoronaphthoic acids.
2002-02-22
Identification of novel Ah receptor agonists using a high-throughput green fluorescent protein-based recombinant cell bioassay.
2002-01-22
Staining electrophoretic gels for laccase and peroxidase activity using 1,8-diaminonaphthalene.
2001-06-01
Patents
Name Type Language
NSC-6081
Preferred Name English
1,8-NAPHTHALENEDIAMINE
MI  
Systematic Name English
1,8-NAPHTHALENEDIAMINE [MI]
Common Name English
1,8-DIAMINONAPHTHALENE
Systematic Name English
Code System Code Type Description
FDA UNII
IKA7029YH9
Created by admin on Mon Mar 31 18:55:28 GMT 2025 , Edited by admin on Mon Mar 31 18:55:28 GMT 2025
PRIMARY
WIKIPEDIA
1,8-DIAMINONAPHTHALENE
Created by admin on Mon Mar 31 18:55:28 GMT 2025 , Edited by admin on Mon Mar 31 18:55:28 GMT 2025
PRIMARY
EPA CompTox
DTXSID6044432
Created by admin on Mon Mar 31 18:55:28 GMT 2025 , Edited by admin on Mon Mar 31 18:55:28 GMT 2025
PRIMARY
NSC
6081
Created by admin on Mon Mar 31 18:55:28 GMT 2025 , Edited by admin on Mon Mar 31 18:55:28 GMT 2025
PRIMARY
MERCK INDEX
m7727
Created by admin on Mon Mar 31 18:55:28 GMT 2025 , Edited by admin on Mon Mar 31 18:55:28 GMT 2025
PRIMARY Merck Index
PUBCHEM
68067
Created by admin on Mon Mar 31 18:55:28 GMT 2025 , Edited by admin on Mon Mar 31 18:55:28 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-529-8
Created by admin on Mon Mar 31 18:55:28 GMT 2025 , Edited by admin on Mon Mar 31 18:55:28 GMT 2025
PRIMARY
CAS
479-27-6
Created by admin on Mon Mar 31 18:55:28 GMT 2025 , Edited by admin on Mon Mar 31 18:55:28 GMT 2025
PRIMARY
MESH
C508862
Created by admin on Mon Mar 31 18:55:28 GMT 2025 , Edited by admin on Mon Mar 31 18:55:28 GMT 2025
PRIMARY