ChemicalBook--->CAS DataBase List--->5466-89-7

5466-89-7

5466-89-7 Structure

5466-89-7 Structure
IdentificationBack Directory
[Name]

3',4'-DIHYDROXY-2-METHYLPROPIOPHENONE
[CAS]

5466-89-7
[Synonyms]

U-0521
U-0521,98+%
U0521,U 0521
3’,4’-dihydroxy-isobutyrophenon
3’,4’-dihydroxyisobutyrophenone
3’,4’-dihydroxy-2-methyl-propiophenon
3',4'-DIHYDROXY-2-METHYLPROPIOPHENONE
3',4'-Dihydroxy-α-methylpropiophenone
1-(3,4-dihydroxyphenyl)-2-methyl-1-propanon
1-(3,4-Dihydroxyphenyl)-2-methylpropan-1-one
1-Propanone, 1-(3,4-dihydroxyphenyl)-2-methyl-
[Molecular Formula]

C10H12O3
[MDL Number]

MFCD00211220
[MOL File]

5466-89-7.mol
[Molecular Weight]

180.2
Chemical PropertiesBack Directory
[Melting point ]

79-81℃
[Boiling point ]

372.2±27.0 °C(Predicted)
[density ]

1.191±0.06 g/cm3(Predicted)
[RTECS ]

NQ5605000
[storage temp. ]

-20°C Freezer
[solubility ]

Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
[form ]

White solid.
[pka]

8.77±0.31(Predicted)
[color ]

Off-White to Pale Beige
Hazard InformationBack Directory
[Uses]

U-0521 is an extraneuronal COMT uptake inhibitor.
[Definition]

ChEBI: U 0521 is a member of acetophenones.
[in vivo]

U-0521 (i.p.; 0-250 mg/kg; 10 min) inhibits COMT activity in a dose-dependent manner. 50% inhibition of enzyme activity is obtained at 90 mg/kg and maximum inhibition of 90% is obtained at 250 mg/kg[1].

Animal Model:Male Sprague-Dawley rats (180-250 g)[1]
Dosage:0-250 mg/kg
Administration:i.p.; 10 min
Result:Inhibited COMT activity in a dose-dependent manner. 50% inhibition of enzyme activity was obtained at 90mg/kg and maximum inhibition of 90% was obtained at 250 mg/kg.
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