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1-(4-chlorophenyl)-4-morpholin-4-yl-5H-imidazol-2-one

1-(4-chlorophenyl)-4-morpholin-4-yl-5H-imidazol-2-one Structure
  • ₹0
  • Product name: 1-(4-chlorophenyl)-4-morpholin-4-yl-5H-imidazol-2-one
  • CAS: 188116-07-6
  • MF: C13H14ClN3O2
  • MW: 279.72
  • EINECS:200-256-5
  • MDL Number:MFCD18450225
  • Synonyms:1-(4-chlorophenyl)-4-morpholin-4-yl-5H-imidazol-2-one;Imepitoin;1-(4-CHLOROPHENYL)-4-MORPHOLINO-1H-IMIDAZOL-2(5H)-ONE;1-(4-Chlorophenyl)-1,5-dihydro-4-(4-morpholinyl)-2H-imidazol-2-one;2H-Imidazol-2-one,1-(4-chlorophenyl)-1,5-dihydro-4-(4-morpholinyl)-;Imepitoin 1-(4-Chlorophenyl)-1,5-dihydro-4-(4-morpholinyl)-2H-imidazol-2-one;AWD 131-138, >=98%;3-(4-chlorophenyl)-5-morpholin-4-yl-4H-imidazol-2-one
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Melting point :264℃ (ethanol )
Boiling point :421.8±55.0 °C(Predicted)
Density :1.42±0.1 g/cm3(Predicted)
storage temp. :2-8°C
solubility :DMF:10.0(Max Conc. mg/mL);35.75(Max Conc. mM)
DMSO:17.5(Max Conc. mg/mL);62.56(Max Conc. mM)
DMSO:PBS (pH 7.2) (1:1):0.5(Max Conc. mg/mL);1.79(Max Conc. mM)
Ethanol:1.13(Max Conc. mg/mL);4.02(Max Conc. mM) form :A crystalline solid
pka :4.39±0.20(Predicted)
color :White to off-white

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
Precautionary statements:
P201 Obtain special instructions before use.
P202 Do not handle until all safety precautions have been read and understood.
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P308+P313 IF exposed or concerned: Get medical advice/attention.
P405 Store locked up.
P501 Dispose of contents/container to..…

Description

AWD 131-138 is a partial agonist of the GABAA receptor that acts at the benzodiazepine binding site, dose-dependently stimulating GABA currents with a threshold of 0.3-1.0 μM. This effect is blocked by the benzodiazepine antagonist flumazenil . AWD 131-138 displays a broad spectrum of anticonvulsant activity in diverse seizure and epilepsy models without a tendency toward tolerance or abuse. It has a superior pharmacokinetic profile in dogs vs. humans.

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