Home Aminos 2,6-Diaminoanthraquinone

2,6-Diaminoanthraquinone

CAS No.:
131-14-6
Catalog Number:
AG000VAI
Molecular Formula:
C14H10N2O2
Molecular Weight:
238.2414
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$25
- +
100g
98%
In Stock USA
United States
$75
- +
500g
98%
In Stock USA
United States
$350
- +
Product Description
Catalog Number:
AG000VAI
Chemical Name:
2,6-Diaminoanthraquinone
CAS Number:
131-14-6
Molecular Formula:
C14H10N2O2
Molecular Weight:
238.2414
MDL Number:
MFCD00001234
IUPAC Name:
2,6-diaminoanthracene-9,10-dione
InChI:
InChI=1S/C14H10N2O2/c15-7-1-3-9-11(5-7)14(18)10-4-2-8(16)6-12(10)13(9)17/h1-6H,15-16H2
InChI Key:
WQOWBWVMZPPPGX-UHFFFAOYSA-N
SMILES:
Nc1ccc2c(c1)C(=O)c1c(C2=O)cc(cc1)N
EC Number:
205-013-7
UNII:
3DY0EUZ2ZM
NSC Number:
39935
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:
1.5  
Literature
Title Journal
Determination of the optical GAP in thin films of amorphous dilithium phthalocyanine using the Tauc and Cody models. Molecules (Basel, Switzerland) 20120824
Study of preferential solvation of 2,6-diaminoanthraquinone in binary mixtures by absorption and fluorescence studies. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20080801
Solvent polarity induced structural changes in 2,6-diamino-9,10-anthraquinone dye. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20080101
Photophysical behaviour of 2,6-diaminoanthraquinone in different solvents and at various pH. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20071101
Long-wavelength analogue of PRODAN: synthesis and properties of Anthradan, a fluorophore with a 2,6-donor-acceptor anthracene structure. The Journal of organic chemistry 20061222
Prediction of genotoxicity of chemical compounds by statistical learning methods. Chemical research in toxicology 20050601
A homogeneous time-resolved fluorescence detection of telomerase activity. Analytical biochemistry 20041001
Nanowells on silica particles in water containing long-distance porphyrin heterodimers. Journal of the American Chemical Society 20030903
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