Acetylglycinamide chloral hydrate: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
 
CSV import
 
(One intermediate revision by the same user not shown)
Line 25: Line 25:
[[Category:Amides]]
[[Category:Amides]]
{{Chem-stub}}
{{Chem-stub}}
{{No image}}
__NOINDEX__

Latest revision as of 03:23, 17 March 2025

Acetylglycinamide chloral hydrate (ACH) is a chemical compound with the molecular formula C4H7Cl3N2O3. It is a derivative of chloral hydrate and glycinamide, and is used in various chemical synthesis processes.

Chemical Structure[edit]

The chemical structure of acetylglycinamide chloral hydrate consists of a chloral group attached to a glycinamide group via an acetyl linkage. This structure gives ACH its unique chemical properties, including its reactivity and solubility.

Synthesis[edit]

Acetylglycinamide chloral hydrate is synthesized through a reaction between chloral hydrate and glycinamide. The reaction is typically carried out in an organic solvent such as dichloromethane or ethyl acetate, and may be catalyzed by an acid or base.

Properties[edit]

ACH is a white, crystalline solid at room temperature. It is soluble in water and most organic solvents. It has a melting point of approximately 150-155 degrees Celsius.

Applications[edit]

Acetylglycinamide chloral hydrate is primarily used in chemical synthesis. It is a versatile reagent that can be used in a variety of reactions, including condensation reactions, addition reactions, and substitution reactions. It is also used in the synthesis of certain pharmaceuticals and biologically active compounds.

Safety[edit]

Like many chemical compounds, ACH should be handled with care. It can cause irritation to the skin and eyes, and may be harmful if swallowed or inhaled. Appropriate safety measures should be taken when handling this compound.

See Also[edit]

This article is a stub related to chemistry. You can help WikiMD by expanding it!