117-12-4

  • Product Name:1,5-Dihydroxyanthraquinone
  • Molecular Formula:C14H8O4
  • Purity:99%
  • Molecular Weight:240.215
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Product Details;

CasNo: 117-12-4

Molecular Formula: C14H8O4

Quality Manufacturer Supply High Purity 1,5-Dihydroxyanthraquinone 117-12-4 Efficient Shipping

  • Molecular Formula:C14H8O4
  • Molecular Weight:240.215
  • Vapor Pressure:8.21E-09mmHg at 25°C 
  • Melting Point:279 °C (dec.)(lit.) 
  • Refractive Index:1.732 
  • Boiling Point:452.7 °C at 760 mmHg 
  • PKA:6.42±0.20(Predicted) 
  • Flash Point:241.7 °C 
  • PSA:74.60000 
  • Density:1.54 g/cm3 
  • LogP:1.87320 

1,5-Dihydroxyanthraquinone(Cas 117-12-4) Usage

Chemical Properties

Yellow to Green Solid

Uses

1,5-Dihydroxyanthraquinone is an anthraquinone derivative with suppressive effects against nitric oxide (NO) synthase. Potential antimalarial agent. Used in studies as a potential competitive non-peptidic inhibitor of HIV-1 protei nase.

Definition

ChEBI: A dihydroxyanthraquinone that is anthracene-9,10-dione substituted by hydroxy groups at positions 1 and 5.

Purification Methods

Purify anthrarufin by column chromatography on silica gel with CHCl3/Et2O as eluent, followed by recrystallisation from acetone. Alternatively recrystallise it from glacial acetic acid [Flom & Barbara J Phys Chem 89 4489 1985]. [Beilstein 7 III 2359, 8 IV 3268.]

InChI:InChI=1/C14H8O4/c15-9-5-1-3-7-11(9)14(18)8-4-2-6-10(16)12(8)13(7)17/h1-6,15-16H

117-12-4 Relevant articles

Efficient reductive Claisen rearrangement of prop-2’-enyloxyanthraquinones and 2’-chloroprop-2’-enyloxyanthraquinones with iron powder in ionic liquids

Nadali, Samaneh,Khoshroo, Ali,Aghapour, Ghasem

, p. 883 - 895 (2018)

A rapid and selective iron-mediated redu...

Surface-enhanced Raman scattering of 1,5-dihydroxyanthraquinone in silver sol

S.Edwin Jayaraj, V. Ramakrishnan

, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy Volume 51, Issue 6, June 1995, Pages 979-983

Surface-enhanced Raman scattering studies on 1,5-dihydroxyanthraquinone (1,5-DHAQ) were undertaken to elucidate the molecular orientation on the silver particles and the enhancement mechanism. The 1,5-DHAQ molecule is adsorbed through its coordinating sites (CO groups) and it is found to have a stand-on configuration.

Highly selective three-step synthesis of rhein in chloroaluminate molten salt: preclusion of the Hayashi rearrangement

Gonnot, Vanessa,Antheaume, Cyril,Nicolas, Marc,Mioskowski, Charles,Baati, Rachid

experimental part, p. 6205 - 6210 (2010/03/24)

An expeditious, three-step synthesis of ...

Pathway of anthracene modification under simulated solar radiation

Mallakin, Ali,George Dixon,Greenberg, Bruce M.

, p. 1435 - 1441 (2007/10/03)

Exposure of polycyclic aromatic hydrocar...

117-12-4 Process route

1,5-bis-diacetoxyboranyloxy-anthraquinone
87965-33-1

1,5-bis-diacetoxyboranyloxy-anthraquinone

1,5-dihydroxyanthraquinone
117-12-4

1,5-dihydroxyanthraquinone

metaboric acid
13460-50-9

metaboric acid

acetic acid
64-19-7,77671-22-8

acetic acid

Conditions
Conditions Yield
 
 
anthracene
120-12-7

anthracene

1,5-dihydroxyanthraquinone
117-12-4

1,5-dihydroxyanthraquinone

1-hydroxyanthraquinone
129-43-1

1-hydroxyanthraquinone

1,4-dihydroxy-9,10-anthracenedione
81-64-1,103220-12-8

1,4-dihydroxy-9,10-anthracenedione

1,8-dihydroxy-9,10-anthracenedione
117-10-2

1,8-dihydroxy-9,10-anthracenedione

Conditions
Conditions Yield
In water; Further byproducts given; Formation of xenobiotics; simulated solar irradiation;
 

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