Basic information Safety Supplier Related

3'-Hydroxypropiophenone

Basic information Safety Supplier Related

3'-Hydroxypropiophenone Basic information

Product Name:
3'-Hydroxypropiophenone
Synonyms:
  • 1-(3-hydroxyphenyl)propan-1-one
  • 1-Propanone,1-(3-hydroxyphenyl)-
  • 3-HYDROXY PROPIOPHENONE
  • 3'-HYDROXYPROPIOPHENONE
  • Metaraminol Bitartrate Impurity 13
  • 3'-Hydroxypropiophenone
  • Metaraminol bitartrate Impurity 44
  • Metaramine bitartrate Impurity 44
CAS:
13103-80-5
MF:
C9H10O2
MW:
150.17
EINECS:
236-027-1
Mol File:
13103-80-5.mol
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3'-Hydroxypropiophenone Chemical Properties

Melting point:
82 °C
Boiling point:
288.9±23.0 °C(Predicted)
Density 
1.104±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form 
Solid
pka
9.09±0.10(Predicted)
color 
Off-White to Beige
CAS DataBase Reference
13103-80-5(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HS Code 
2914500090
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3'-Hydroxypropiophenone Usage And Synthesis

Uses

1-?(3-?Hydroxyphenyl)?-?1-?propanone is a reactant used to synthesize tricyclic fused pyridines, a family of alkaloids with antimalarial activity.

Preparation

Preparation by diazotization of m-aminopropiophenone, followed by decomposition of the diazonium salt obtained, (71%)
Also obtained by saponification of 3-acetoxypropiophenone (b.p.2 127–128°) with refluxing 10% sodium hydroxide for 2–3 h (83%)
Also obtained by reductive deamination of 2-amino-5-hydroxypropiophenone (diazotization, followed by decomposition of the diazonium salt formed with copper powder in ethanol)
Also obtained by reaction of ethylmagnesium bromide with 3-hydroxy-N, N-diethylbenzamide in refluxing n-butyl ether for 4 h (75%)
Also obtained by treatment of 3-methoxypropiophenone (b.p.0.05 70–76°) with pyridinium chloride at 210° for 30 min (85%)
Also obtained by treatment of 1-hydroxy-1-(3-hydroxyphenyl)propane (m.p. 105–107°) with DDQ in dioxane for 72 h (97%).

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