6341-67-9

Usage

Chemical class

Imidazolidines

Use

Pharmaceutical intermediate

Molecular weight

170.16 g/mol

Physical state

White crystalline solid

Solubility

Slightly soluble in water

Biological activities

Anticonvulsant and sedative effects

Potential applications

Corrosion inhibitor, additive in bio-based polymers

Versatility

Wide range of applications in various fields

Upstream product

• 18968-51-9 1,2-O-isopropylidene-3-O-methyl-α-D-xylo-pentodialdo-1,4-furanose 
• 77-71-4 5,5-dimethyl-imidazolidine-2,4-dione 
• 75-36-5 acetyl chloride 
• 67005-72-5 3-acetyl-5,5-dimethyl-imidazolidine-2,4-dione 
• 79662-84-3 (1-Cyan-1-methylethyl)harnstoff 
• 71-43-2 benzene 
• 108-24-7 acetic anhydride 

Downstream Products

• 102617-81-2 3-Acetyl-4,4-dimethyl-2,5-dioxo-imidazolidine-1-carbonitrile 

Relevant academic research and scientific papers

On the chlorenium source in the asymmetric chlorolactonization reaction

N-Acylated N-chlorohydantoins are shown to be competent chlorenium sources in the (DHQD)2PHAL-mediated asymmetric chlorolactonization. The derivatives demonstrate the exact role of the N1 and N3 chlorine atoms in the parent dichlorohydantoins w

APPLICATION OF THE BUCHERER REACTION TO CARBOHYDRATE DERIVATIVES

The Bucerer reaction of carbohydrate derivatives having a free carbonyl group proceeds normally, giving mainly the expected spiro-hydantoin derivatives.With derivatives having a free aldehydo group attached to an acetal ring in an α-position, the acetal ring is opened via an elimination reaction yielding unsaturated hydantoin derivatives.These reactions were studied using 1,2:5,6-di-O-isopropylidene-α-D-ribo-hexofuranos-3-ulose, 2,3:4,5-di-O-isopropylidene-D-arabinose, -D-ribose, and -D-xylose, 2,3:5,6-di-O-isopropylidene-α-D-mannofuranose, 1,2-O-isopropylidene-3-O-methyl-α-D-xylo-pentodialdo-1,4-mannofuranose, 1,2:3,4-di-O-isopropylidene-α-D-galacto-hexodialdo-1,5-pyranose, and 2,3:4,5-di-O-isopropylidene-β-D-arabino-hexosulo-2,6-pyranose.