117-78-2 | Anthraquinone-2-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$17.00	$12.00
5g	95%	in stock	$23.00	$17.00
25g	95%	in stock	$55.00	$38.00
100g	95%	in stock	$205.00	$144.00

Description

• Catalog Number: AA17305
• Chemical Name: Anthraquinone-2-carboxylic acid
• CAS Number: 117-78-2
• Molecular Formula: C15H8O4
• Molecular Weight: 252.2216
• MDL Number: MFCD00001231
• SMILES: O=C1c2cc(ccc2C(=O)c2c1cccc2)C(=O)O
• NSC Number: 5001

Computed Properties

• Complexity: 428
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 3

Upstream Synthesis Route

9,10-Dioxo-9,10-dihydroanthracene-2-carboxylic acid is a versatile compound commonly used in chemical synthesis. It serves as a key building block in the production of various organic molecules due to its unique structure and reactivity. This compound is frequently employed as a precursor in the synthesis of pharmaceuticals, agrochemicals, and materials for advanced applications. Its functional groups make it ideal for introducing specific chemical moieties through various synthetic reactions, allowing for the creation of complex molecular structures. In addition, 9,10-Dioxo-9,10-dihydroanthracene-2-carboxylic acid can participate in diverse transformations such as esterification, amidation, and coupling reactions, enabling chemists to design and construct intricate molecules with precision and control.

Literature

• Comparison of dispersive liquid-liquid microextraction based on organic solvent and ionic liquid combined with high-performance liquid chromatography for the analysis of emodin and its metabolites in urine samples.

  Journal of separation science 20120101

• Intermolecular and intracomplex photoinduced electron transfer from planar and nonplanar metalloporphyrins to p-quinones.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20111024

• Simultaneous topographic and amperometric membrane mapping using an AFM probe integrated biosensor.

  Biosensors & bioelectronics 20110215

• Potent inhibitor scaffold against Trypanosoma cruzi trans-sialidase.

  Bioorganic & medicinal chemistry 20100215

• Adsorption state and morphology of anthraquinone-2-carboxylic acid deposited from solution onto the atomically-smooth native oxide surface of Al(111) films studied by infrared reflection absorption spectroscopy, X-ray photoelectron spectroscopy, and atomic force microscopy.

  Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20080301

• Antibacterial activity of Tabebuia impetiginosa Martius ex DC (Taheebo) against Helicobacter pylori.

  Journal of ethnopharmacology 20060421

• Selective growth-inhibiting effects of compounds identified in Tabebuia impetiginosa inner bark on human intestinal bacteria.

  Journal of agricultural and food chemistry 20050223

• Anthraquinones isolated from Cassia tora (Leguminosae) seed show an antifungal property against phytopathogenic fungi.

  Journal of agricultural and food chemistry 20041006

• Resolution of overlapped non-absorbing and absorbing solutes using either an absorption null-balance detection window or multivariate deconvolution applied to capillary electrophoresis of anionic surfactants.

  Journal of chromatography. A 20040521

• Synthesis of oligonucleotides with a 2'-cap at the 3'-terminus via reversed phosphoramidites.

  Organic letters 20030206

• Possible cause of G-C-->C-G transversion mutation by guanine oxidation product, imidazolone.

  Chemistry & biology 20010401

• L-proline analogues of anthraquinone-2-carboxylic acid: cytotoxic activity in breast cancer MCF-7 cells and inhibitory activity against topoisomerase I and II.

  Polish journal of pharmacology 20010101

• Cytotoxicity activity of L-proline analogues of anthraquinone-2-carboxylic acid in breast cancer MCF-7 cells.

  Folia histochemica et cytobiologica 20010101