129-44-2 | 1,5-Diaminoanthraquinone

Packsize	Purity	Availability	Price	Discounted Price
25mg	95%(HPLC)	in stock	$31.00	$22.00
250mg	tech	in stock	$39.00	$27.00
5g	>92.0%(N)	in stock	$42.00	$30.00

Description

• Catalog Number: AA44852
• Chemical Name: 1,5-Diaminoanthraquinone
• CAS Number: 129-44-2
• Molecular Formula: C14H10N2O2
• Molecular Weight: 238.2414
• MDL Number: MFCD00001226
• SMILES: Nc1cccc2c1C(=O)c1cccc(c1C2=O)N

Computed Properties

• Complexity: 346
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• XLogP3: 2.6

Literature

• 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