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3,5-Dibenzyloxyacetophenone

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3,5-Dibenzyloxyacetophenone Basic information

Product Name:
3,5-Dibenzyloxyacetophenone
Synonyms:
  • 3',5'-DIBENZYLOXYACETOPHENONE
  • 3,5-DIBENZYLOXYACETOPHENONE
  • 3',5'-DIBENZYLOXYACETPHENONE
  • 3',5'-BIS(BENZYLOXY)ACETOPHENONE
  • 1-[3,5-bis(phenylmethoxy)phenyl]-ethanon
  • 1-[3,5-Bis(benzyloxy)phenyl]ethan-1-one
  • Terbutaline Impurity 1
  • 3',5'-Dibenzyloxyacetophenone 3,5-Dibenzyloxyacetophenone
CAS:
28924-21-2
MF:
C22H20O3
MW:
332.39
EINECS:
249-315-7
Product Categories:
  • Aromatic Acetophenones & Derivatives (substituted)
  • API intermediates
  • Building Blocks for Dendrimers
  • Functional Materials
  • Aromatics
  • C15 to C38
  • Carbonyl Compounds
  • Ketones
  • bc0001
  • 28924-21-2
Mol File:
28924-21-2.mol
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3,5-Dibenzyloxyacetophenone Chemical Properties

Melting point:
60-62 °C (lit.)
Boiling point:
429.52°C (rough estimate)
Density 
1.1079 (rough estimate)
refractive index 
1.6000 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Soluble in dichloromethane, ethyl acetate and methanol
form 
Solid
color 
Off-White to Pale Yellow
InChIKey
KOJXGMJOTRYLBD-UHFFFAOYSA-N
CAS DataBase Reference
28924-21-2(CAS DataBase Reference)
EPA Substance Registry System
Ethanone, 1-[3,5-bis(phenylmethoxy)phenyl]- (28924-21-2)
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Safety Information

Hazard Codes 
Xi
Safety Statements 
24/25
WGK Germany 
3
Hazard Note 
Irritant
TSCA 
Yes
HS Code 
29145090

MSDS

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3,5-Dibenzyloxyacetophenone Usage And Synthesis

Chemical Properties

beige crystalline powder. 

Uses

3,5-Dibenzyloxyacetophenone is used in the synthesis of enantiomerically pure B-ring modified analogs of (-)-epicatechin gallate.

Uses

The product 3,5-dibenzyloxyacetophenone is widely used as intermediate in the production of a pharmaceutical for treatment of obesity, diabetes, glaucoma, AIDS, HIV infection, antiinflammatory effects, and also in the treatment of disorders which result from leukotriene, tranquilizers, hypotensives, diuretics, and antiglaucoma agents.[1]

References

[1] Ganapati D. Yadav,  Omprakash V. Badure. “Selective acylation of 1,3-dibenzyloxybenzene to 3,5-dibenzyloxyacetophenone over cesium modified dodecatungstophosphoric acid (DTP) on clay.” Applied Catalysis A: General 348 1 (2008): Pages 16-25.

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