Basic information Safety Supplier Related

Anthracene-1,4,9,10-tetraol

Basic information Safety Supplier Related

Anthracene-1,4,9,10-tetraol Basic information

Product Name:
Anthracene-1,4,9,10-tetraol
Synonyms:
  • 2,3-DIHYDRO-9,10-DIHYDROXY-1,4-ANTHRAQUINONE
  • N-(3-chloro-9-oxo-2-fluorenyl)-2,2,2-trifluoroacetamide
  • 1,4-DIHYDROXYANTHRAHYDROQUINONE
  • 1,4-DIHYDROXY ANTHRAQUINONE LEUCO COMPOUND
  • 1,4,9,10-TETRAHYDROXYANTHRACENE
  • 1,4,9,10-ANTHRACENETETROL
  • LEUCOQUINIZARIN
  • LEUCO QUINIZARINE
CAS:
476-60-8
MF:
C14H10O4
MW:
242.23
EINECS:
207-507-8
Product Categories:
  • Anthracenes
Mol File:
476-60-8.mol
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Anthracene-1,4,9,10-tetraol Chemical Properties

Melting point:
151 °C
Boiling point:
305.05°C (rough estimate)
Density 
1.1478 (rough estimate)
refractive index 
1.5190 (estimate)
storage temp. 
Sealed in dry,Room Temperature
pka
8.11±0.30(Predicted)
InChI
InChI=1S/C14H10O4/c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18/h1-6,15-18H
InChIKey
BKNBVEKCHVXGPH-UHFFFAOYSA-N
SMILES
C1(O)=C2C(C(O)=C3C(=C2O)C=CC=C3)=C(O)C=C1
CAS DataBase Reference
476-60-8(CAS DataBase Reference)
EPA Substance Registry System
1,4,9,10-Anthracenetetrol (476-60-8)
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Safety Information

RTECS 
OH4742000
HS Code 
2907.29.9000
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Anthracene-1,4,9,10-tetraol Usage And Synthesis

Description

Anthracene-1,4,9,10-tetraol is an important chemical intermediate. It has an important position in the dye industry, can be used in the research and development of pharmaceutical intermediates such as anti-tumor drugs, anti-cancer, etc., and can also be widely used in solvent dyes, disperse dyes, reactive dyes, and vat dye intermediates.

Uses

1,4,9,10-Anthracenetetraone (quinizarindiquinone) derivative is an important electrode material and serves as a potent diphenol reagent for Diels-Alder reactions. In recent years, the anticancer activity of Anthracene-1,4,9,10-tetraol has often been studied separately, and it is often used in the research and use of antitumor drugs and dyes.

Synthesis Reference(s)

Tetrahedron Letters, 19, p. 2937, 1978 DOI: 10.1016/S0040-4039(01)94905-6

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