Basic information Safety Supplier Related

5'-CHLORO-2'-HYDROXY-4'-METHYLACETOPHENONE

Basic information Safety Supplier Related

5'-CHLORO-2'-HYDROXY-4'-METHYLACETOPHENONE Basic information

Product Name:
5'-CHLORO-2'-HYDROXY-4'-METHYLACETOPHENONE
Synonyms:
  • 5'-CHLORO-2'-HYDROXY-4'-METHYLACETOPHENONE
  • 5-CHLORO-2-HYDROXY-4-METHYLACETOPHENONE
  • 4-ACETYL-2-CHLORO-5-HYDROXYTOLUENE
  • 1-(5-CHLORO-2-HYDROXY-4-METHYLPHENYL)ETHANONE
  • 2-ACETYL-4-CHLORO-5-METHYLPHENOL
  • 5'-Chooro-2'-Hydroxy-4'-Methylacetophenone
  • JRH-01005, 1-(5-Chloro-2-hydroxy-4-methylphenyl)ethanone, 97%
  • 4-Acetyl-2-chloro-5-hydroxytoluene 2-Acetyl-4-chloro-5-methylphenol
CAS:
28480-70-8
MF:
C9H9ClO2
MW:
184.62
Product Categories:
  • Ketones
  • Aromatic Acetophenones & Derivatives (substituted)
  • C9
  • Carbonyl Compounds
Mol File:
28480-70-8.mol
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5'-CHLORO-2'-HYDROXY-4'-METHYLACETOPHENONE Chemical Properties

Melting point:
70-73 °C(lit.)
Boiling point:
137 °C / 15mmHg
Density 
1.250±0.06 g/cm3(Predicted)
form 
powder to crystal
pka
9.84±0.23(Predicted)
color 
White to Light yellow
CAS DataBase Reference
28480-70-8(CAS DataBase Reference)
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Safety Information

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

MSDS

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5'-CHLORO-2'-HYDROXY-4'-METHYLACETOPHENONE Usage And Synthesis

Uses

5′-Chloro-2′-hydroxy-4′-methylacetophenone (5-chloro-2-hydroxy-4-methylacetophenone) may be used in the preparation of the following:

  • chalcones, required for the synthesis of novel pyrazoline derivatives
  • 5′-chloro-2′-hydroxy-4′-methyl-3-(2′′-thienyl)acrylophenone
  • 6-chloro-3-hydroxy-7-methyl-2-(2-thienyl)-4H-chromen-4-one, a complexing agent used for the spectrophotometric determination of vanadium(V)

Preparation

Preparation by reaction of acetic acid on 4-chloro-3- methylphenol with boron trifluoride at 70–100° (80–85%).

General Description

5′-chloro-2′-hydroxy-4′-methylacetophenone (5-Chloro-2-hydroxy-4-methylacetophenone) is a hydroxylated aromatic acetophenone. Its iodination by pyridinium iodochloride has been reported to afford 5-chloro-2-hydroxy-3-iodo-4-methylacetophenone.

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