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2,4,4'-TRIHYDROXYBENZOPHENONE

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2,4,4'-TRIHYDROXYBENZOPHENONE Basic information

Product Name:
2,4,4'-TRIHYDROXYBENZOPHENONE
Synonyms:
  • 2,4,4'-Trihydroxybenzophenone 95%
  • (2,4-dihydroxyphenyl)(4-hydroxyphenyl)-methanon
  • 2,4-Dihydroxyphenyl p-hydroxybenzyl ketone
  • Methanone, (2,4-dihydroxyphenyl)(4-hydroxyphenyl)-
  • 2,4,4'-TRIHYDROXYBENZOPHENONE
  • (2,4-DIHYDROXY-PHENYL)-(4-HYDROXY-PHENYL)-METHANONE
  • LABOTEST-BB LT00159581
  • 2,4,4-TRIHYDROXYBENZOPHENONE 98+%
CAS:
1470-79-7
MF:
C13H10O4
MW:
230.22
EINECS:
216-004-2
Product Categories:
  • Building Blocks
  • C13 to C14
  • Benzophenones (for High-Performance Polymer Research)
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks
  • Industrial/Fine Chemicals
  • Functional Materials
  • Reagent for High-Performance Polymer Research
  • C13 to C14
  • Carbonyl Compounds
  • Ketones
Mol File:
1470-79-7.mol
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2,4,4'-TRIHYDROXYBENZOPHENONE Chemical Properties

Melting point:
197-198 °C(lit.)
Boiling point:
332.2°C (rough estimate)
Density 
1.2683 (rough estimate)
refractive index 
1.4977 (estimate)
Water Solubility 
Slightly soluble in water
form 
powder to crystal
pka
7.59±0.35(Predicted)
color 
White to Light yellow to Light orange
CAS DataBase Reference
1470-79-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-24/25
WGK Germany 
3
HS Code 
2914.50.3000

MSDS

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2,4,4'-TRIHYDROXYBENZOPHENONE Usage And Synthesis

Chemical Properties

orange powder or chunks

Uses

2,4,4''-Trihydroxybenzophenone is a small molecule inhibitor of viral replication.

Preparation

Preparation by reaction of 4-hydroxybenzoic acid with resorcinol,
? in the presence of zinc chloride at 160° (Nencki reaction);
? in the presence of zinc chloride and phosphorous oxychloride for 4 days at r.t. (78%);
in the presence of zinc chloride and a mixture of polyphosphoric acid/85% phosphoric acid (60:40) at 27°. Then, during 2 h, phosphorous trichloride was added between 27° and 37° and the mixture heated at 60° for 16 h (quantitative yield);
? in the presence of hydrofluoric acid at 75° in an autoclave.

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