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