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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

Molecular Formula C10H10N2
Molecular Weight 158.1998
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Staining electrophoretic gels for laccase and peroxidase activity using 1,8-diaminonaphthalene.
2001 Jun 1
Tetraaminoperylenes: their efficient synthesis and physical properties.
2002 Aug 16
Synthesis of mono- and difluoronaphthoic acids.
2002 Feb 22
Identification of novel Ah receptor agonists using a high-throughput green fluorescent protein-based recombinant cell bioassay.
2002 Jan 22
A PVC-based 1,8-diaminonaphthalen electrode for selective determination of vanadyl ion.
2003 Jul 4
Unexpected reaction pathways in the reaction of alkoxyalkynylchromium(0) carbenes with aromatic dinucleophiles.
2003 Oct 17
Waste-free and facile solid-state protection of diamines, anthranilic acid, diols, and polyols with phenylboronic acid.
2003 Sep 5
Insignificance of P-H...P hydrogen bonding: structural chemistry of neutral and protonated 1,8-di(phosphinyl)naphthalene.
2004 Dec 8
Novel photochromic spiroheterocyclic molecules via oxidation of 1,8-diaminonaphthalene.
2005 Apr 14
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005 Jun
Visible colorimetric fluoride ion sensors.
2005 Jun 23
A picosecond time-resolved study on prototropic reactions of electronically excited 1,5- and 1,8-diaminonaphthalenes in aqueous solution.
2005 Mar
Ground and excited states proton transfer reactions of 1,8-diaminonaphthalene in perchloric acid solutions.
2005 Sep
Chimeric antibody-binding Vitreoscilla hemoglobin (VHb) mediates redox-catalysis reaction: new insight into the functional role of VHb.
2006 Aug 22
Group 4 catalysts for ethene polymerization containing tetradentate salicylaldiminato ligands.
2006 Dec 14
Efficient solvent-free syntheses of [2]- and [4]rotaxanes.
2008
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 Sep
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 Apr
Antimicrobial active macrocyclic complexes of Cr(III), Mn(III) and Fe(III) with their spectroscopic approach.
2009 Aug
N,N'-Dineopentyl-naphthalene-1,8-diamine.
2009 Dec 4
Synthesis and spectroscopic studies on complexes of N,N'-bis-(2-pyridinecarboxaldimine)-1,8-diaminonaphthalene (L); DNA binding studies on Cu(II) complex.
2009 Jan
Biologically active macrocyclic complexes derived from diaminonaphthalene and glyoxal: Template synthesis and spectroscopic approach.
2009 Jun
Structural, magnetic, electrochemical, catalytic, DNA binding and cleavage studies of new macrocyclic binuclear copper(II) complexes.
2009 Mar
Structural, electrochemical, phosphate-hydrolysis, DNA binding and cleavage studies of new macrocyclic binuclear nickel(II) complexes.
2010 Apr 28
Chiral boronate derivatives via catalytic enantioselective conjugate addition of Grignard reagents on 3-boronyl unsaturated esters and thioesters.
2010 Apr 28
Template synthesis, spectroscopic, antibacterial, and antifungal studies of trivalent transition metal ion macrocyclic complexes.
2010 Aug
Antibacterial and antifungal studies of macrocyclic complexes of trivalent transition metal ions with their spectroscopic approach.
2010 Feb
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 Feb 19
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:51:49 GMT 2023
Edited
by admin
on Fri Dec 15 17:51:49 GMT 2023
Record UNII
IKA7029YH9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,8-NAPHTHALENEDIAMINE
MI  
Systematic Name English
1,8-NAPHTHALENEDIAMINE [MI]
Common Name English
NSC-6081
Code English
1,8-DIAMINONAPHTHALENE
Systematic Name English
Code System Code Type Description
FDA UNII
IKA7029YH9
Created by admin on Fri Dec 15 17:51:49 GMT 2023 , Edited by admin on Fri Dec 15 17:51:49 GMT 2023
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WIKIPEDIA
1,8-DIAMINONAPHTHALENE
Created by admin on Fri Dec 15 17:51:49 GMT 2023 , Edited by admin on Fri Dec 15 17:51:49 GMT 2023
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EPA CompTox
DTXSID6044432
Created by admin on Fri Dec 15 17:51:49 GMT 2023 , Edited by admin on Fri Dec 15 17:51:49 GMT 2023
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NSC
6081
Created by admin on Fri Dec 15 17:51:49 GMT 2023 , Edited by admin on Fri Dec 15 17:51:49 GMT 2023
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MERCK INDEX
m7727
Created by admin on Fri Dec 15 17:51:49 GMT 2023 , Edited by admin on Fri Dec 15 17:51:49 GMT 2023
PRIMARY Merck Index
PUBCHEM
68067
Created by admin on Fri Dec 15 17:51:49 GMT 2023 , Edited by admin on Fri Dec 15 17:51:49 GMT 2023
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ECHA (EC/EINECS)
207-529-8
Created by admin on Fri Dec 15 17:51:49 GMT 2023 , Edited by admin on Fri Dec 15 17:51:49 GMT 2023
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CAS
479-27-6
Created by admin on Fri Dec 15 17:51:49 GMT 2023 , Edited by admin on Fri Dec 15 17:51:49 GMT 2023
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MESH
C508862
Created by admin on Fri Dec 15 17:51:49 GMT 2023 , Edited by admin on Fri Dec 15 17:51:49 GMT 2023
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