151271-08-8

  • Product Name:imidazenil
  • Molecular Formula:C18H12 Br F N4 O
  • Molecular Weight:399.222
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Product Details

Purity:99%

Factory Supply Industrial Grade imidazenil 151271-08-8 with Best Price

  • Molecular Formula:C18H12 Br F N4 O
  • Molecular Weight:399.222
  • Vapor Pressure:9.25E-14mmHg at 25°C 
  • Boiling Point:587°Cat760mmHg 
  • PKA:15.37±0.40(Predicted) 
  • Flash Point:308.8°C 
  • PSA:73.27000 
  • Density:1.67g/cm3 
  • LogP:3.35970 

imidazenil(Cas 151271-08-8) Usage

Side effects

When taken by mouth: Ostarine is possibly unsafe. It might cause liver damage and other serious side effects such as heart attack.

Synthesis

The synthesis of?imidazenil is as follows:A mixture of 3 g (7.5 mmol) of 6-(2-bromophenyl)-8-fluoro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid, 300 mL of methylene chloride and 2.25 g (10.8 mmol) of phosphorus pentachloride was stirred at room temperature for 2 hours. Ammonia gas was then introduced until the mixture was basic. After layering with 20 mL of concentrated aqueous ammonia, the mixture was stirred for 15 minutes. The methylene chloride was washed with water, dried and evaporated. The residue was crystallized from ethanol/water to yield 2.4 g of product having the above formula. A second crop of 0.4 g was obtained from the mother liquor for a total yield of 2.8 g. For analysis, a sample of the product was recrystallized from methylene chloride/ethanol and had m.p. 298°-299° C.

InChI:InChI=1/C18H12BrFN4O/c19-13-4-2-1-3-11(13)16-12-7-10(20)5-6-14(12)24-9-23-17(18(21)25)15(24)8-22-16/h1-7,9H,8H2,(H2,21,25)

151271-08-8 Relevant articles

Synthesis of iodine-123 labelled analogues of imidazenil and ethyl-imidazenil for studying benzodiazepine receptors using SPECT

Katsifis, Andrew,Mattner, Filomena,Dikic, Branko,Najdovski, Ljubco,Kassiou, Michael

, p. 1121 - 1132 (2007/10/03)

The [123I]iodinated analogues of the ben...

Benzodiazepines and compositions for treating anxiety and panic disorders, and idiopathic and psychomotor epilepsy

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, (2008/06/13)

The present invention is directed to imi...

151271-08-8 Process route

6-(2-bromophenyl)-8-fluoro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid
153874-00-1

6-(2-bromophenyl)-8-fluoro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid

Imidazenil
151271-08-8

Imidazenil

Conditions
Conditions Yield
With ammonium hydroxide; phosphorus pentachloride; Yield given. Multistep reaction; 1.) CH2Cl2, RT, 2 h, 2.) CH2Cl2, 15 min;
With phosphorus pentachloride; ammonia; In dichloromethane;
(2-amino-5-fluorophenyl)(2-bromophenyl)methanone
153873-94-0

(2-amino-5-fluorophenyl)(2-bromophenyl)methanone

Imidazenil
151271-08-8

Imidazenil

Conditions
Conditions Yield
Multi-step reaction with 5 steps
1: 88 percent / tetrahydrofuran / 24 h
2: 71 percent / NH2NH2*H2O / methanol / 24 h
3: 1.) potassium tert-butoxide, diethyl chlorophosphate / 1.) THF, from -20 deg C to 10 deg C, 2.) THF, from -20 deg C to RT, 1.5 h
4: 90 percent / 6 N HCl / 24 h / 90 °C
5: 1.) PCl5, 2.) NH3 (gas), NH4OH / 1.) CH2Cl2, RT, 2 h, 2.) CH2Cl2, 15 min
With hydrogenchloride; ammonium hydroxide; phosphorus pentachloride; potassium tert-butylate; diethyl chlorophosphate; hydrazine hydrate; In tetrahydrofuran; methanol;

151271-08-8 Upstream products

  • 153874-00-1
    153874-00-1

    6-(2-bromophenyl)-8-fluoro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid

  • 153873-94-0
    153873-94-0

    (2-amino-5-fluorophenyl)(2-bromophenyl)methanone

  • 153873-96-2
    153873-96-2

    5-(2-bromophenyl)-7-fluoro-1,3-dihydro-1,4-benzodiazepine-2-one

  • 153873-99-5
    153873-99-5

    6-(2-bromophenyl)-8-fluoro-4H-imidazo[1,5-a][1,4]benzo-diazepine-3-carboxylic acid ethyl ester

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