2-Imidazolidone - Anhydrous

CAS : 120-93-4

Ref. 3D-FI47232

Informations sur le produit

• Nom: 2-Imidazolidone - Anhydrous
• Synonymes: N,N'-Ethyleneurea, 1,3-Ethyleneurea, 2-Imidazaolidone, 2-Imidazolidinone, 2-Imidazolidinone, Pract., 2-Imidazolidon, 2-Imidazolidona, 2-Imidazolidone, 2-Oxoimidazolidine, Cy 100, Ethylene urea, Ethyleneurea, Ethyleneurea hemihydrate, Imidazolid-2-One, Imidazolidin-2-One, Imidazolidinone, Imidazolidone, Katalin CE, N,N'-Aethylenharnstoff, Nsc 21314, Nsc 3338, Sd 6073, Urea - Ethene (1:1), Urea, N,N'-(1,2-ethanediyl)-, Urea, ethylene-

Description

2-Imidazolidone - Anhydrous is an organic compound that is used in the synthesis of glycol ethers. It has been shown to be a potent inhibitor of renal fibrosis in vivo and its pharmacokinetic properties have been studied in a rat model. 2-Imidazolidone - Anhydrous has also been shown to inhibit the production of proinflammatory cytokines and reduce light emission. It is a structural analog of imidazolidinones, which are known to possess antiinflammatory activity. 2-Imidazolidone - Anhydrous can be synthesized by reacting trifluoroacetic acid with an aromatic hydroxyl group and two nitrogen atoms. The major metabolic pathways for this compound include oxidation, reduction, hydrolysis, and conjugation with glucuronic acid. 2-Imidazolidone - Anhydrous reacts with water molecules to form hydrogen peroxide and molecular oxygen gas. This reaction is catalyzed

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 86.09 g/mol
• Formule: C₃H₆N₂O
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder
• InChI: InChI=1S/C3H6N2O/c6-3-4-1-2-5-3/h1-2H2,(H2,4,5,6)
• Code InChI: InChIKey=YAMHXTCMCPHKLN-UHFFFAOYSA-N
• SMILES: O=C1NCCN1