Home Aminos 1,5-Diaminoanthraquinone

1,5-Diaminoanthraquinone

CAS No.:
129-44-2
Catalog Number:
AG000YRG
Molecular Formula:
C14H10N2O2
Molecular Weight:
238.2414
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
25mg
95%(HPLC)
In Stock USA
United States
$46
- +
100mg
95%(HPLC)
In Stock USA
United States
$72
- +
1g
95%(HPLC)
In Stock USA
United States
$151
- +
Product Description
Catalog Number:
AG000YRG
Chemical Name:
1,5-Diaminoanthraquinone
CAS Number:
129-44-2
Molecular Formula:
C14H10N2O2
Molecular Weight:
238.2414
MDL Number:
MFCD00001226
IUPAC Name:
1,5-diaminoanthracene-9,10-dione
InChI:
InChI=1S/C14H10N2O2/c15-9-5-1-3-7-11(9)14(18)8-4-2-6-10(16)12(8)13(7)17/h1-6H,15-16H2
InChI Key:
VWBVCOPVKXNMMZ-UHFFFAOYSA-N
SMILES:
Nc1cccc2c1C(=O)c1cccc(c1C2=O)N
EC Number:
204-947-2
UNII:
3ZXX3HK358
Properties
Complexity:
346  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
238.074g/mol
Formal Charge:
0
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
238.246g/mol
Monoisotopic Mass:
238.074g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
86.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.6  
Literature
Title Journal
1,5-Diamino-2,6-dibromo-9,10-anthraquinone. Acta crystallographica. Section E, Structure reports online 20120301
Construction of an organic crystal structural model based on combined electron and powder X-ray diffraction data and the charge flipping algorithm. Ultramicroscopy 20110601
Molecular recognition of 1,5 diamino anthraquinone by p-tert-butyl-calix(8)arene. Journal of fluorescence 20100901
Estrogenic activity of anthraquinone derivatives: in vitro and in silico studies. Chemical research in toxicology 20100816
Patterned growth of vertically aligned organic nanowire waveguide arrays. ACS nano 20100323
Preferential solvation studies of 1, 5-diaminoanthraquinone in binary liquid mixtures. Journal of fluorescence 20100101
Estimation of first excited singlet-state dipole moments of aminoanthraquinones by solvatochromic method. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20090401
Vertical organic nanowire arrays: controlled synthesis and chemical sensors. Journal of the American Chemical Society 20090311
Valence-state analysis through spectroelectrochemistry in a series of quinonoid-bridged diruthenium complexes [(acac)(2)Ru(mu-L)Ru(acac)(2)](n) (n=+2, +1, 0, -1, -2). Chemistry (Weinheim an der Bergstrasse, Germany) 20080101
Productive synthesis and properties of polydiaminoanthraquinone and its pure self-stabilized nanoparticles with widely adjustable electroconductivity. Chemistry (Weinheim an der Bergstrasse, Germany) 20070101
Prediction of genotoxicity of chemical compounds by statistical learning methods. Chemical research in toxicology 20050601
Electronic absorption spectra of amino substituted anthraquinones and their interpretation using the ZINDO/S and AM1 methods. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20030501
Properties