What is the empirical formula of c4h6n2?

What is the empirical formula of c4h6n2?


What is the molecular weight of imidazole?

68.077 g/mol
Imidazole/Molar mass

How do you prepare imidazole?

Imidazole-HCl Buffer (0.05 M, pH 7.0) Preparation and Recipe

  1. Prepare 800 mL of distilled water in a suitable container.
  2. Add 3.404 g of Imidazole to the solution.
  3. Add 886 mg of HCl to the solution.
  4. Adjust solution to desired pH using HCl (typically pH ≈ 7.0).

Is c4h6n2 aromatic?

1-Methylimidazole or N-methylimidazole is an aromatic heterocyclic organic compound with the formula CH3C3H3N2.

What is the molar mass of potassium carbonate?


Which is the imidazole antifungal?

Ketoconazole topical (Nizoral) Ketoconazole is an imidazole broad-spectrum antifungal agent; it inhibits the synthesis of ergosterol, causing cellular components to leak, resulting in death of fungal cells.

What are the side effects of imidazole?

The imidazoles given PO result in few adverse effects, but nausea, vomiting, and hepatic dysfunction can develop.

Does imidazole affect pH?

Adding imidazole to your buffer, will change the pH of the solution. Double check the pH of the solution after adding imidazole. If there is a high level of contaminant, the imidazole in the equilibration buffer can be increased to 50 – 75 mM.

Which is the correct formula for the compound imidazole?

Imidazole is an organic compound with the formula C 3N 2H 4. It is a white or colourless solid that is soluble in water, producing a mildly alkaline solution. In chemistry, it is an aromatic heterocycle, classified as a diazole, and has non-adjacent nitrogen atoms.

What happens to dialkyl imidazolium in 1-methylimidazole?

1-Methylimidazole alkylates to form dialkyl imidazolium salts. Depending on the alkylating agent and the counteranion, various ionic liquids result, e.g. 1-butyl-3-methylimidazolium hexafluorophosphate (“BMIMPF 6 “):

How are imidazoles prepared from an aldimine in situ?

Amphoterism. The Van Leusen Imidazole Synthesis allows the preparation of imidazoles from aldimines by reaction with tosylmethyl isocyanide (TosMIC). The reaction has later been expanded to a two-step synthesis in which the aldimine is generated in situ: the Van Leusen Three-Component Reaction (vL-3CR).

How is imidazole produced in a photolysis reaction?

Imidazole can be synthesized by the photolysis of 1-vinyltetrazole. This reaction will give substantial yields only if the 1-vinyltetrazole is made efficiently from an organotin compound, such as 2-tributylstannyltetrazole. The reaction, shown below, produces imidazole when R 1 = R 2 = R 3 = hydrogen.

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