28115-25-5

Basic information

• Product Name: 3a,6a-dimethyltetrahydroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione
• Synonyms: 3a,6a-dimethylperhydroimidazo[4,5-d]imidazole-2,5-dione; 3a,6a-Dimethyltetrahydroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione; Imidazo[4,5-d]imidazole-2,5(1H,3H)-dione, tetrahydro-3a,6a-dimethyl-; 3α,6α-Dimethylglycoluril; 3a,6a-Dimethylglycouril
• CAS NO: 28115-25-5
• Molecular Formula: C₆H₁₀N₄O₂
• Molecular Weight: 170.1692
• Mol File: 28115-25-5.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 602.6°C at 760 mmHg
• Flash Point: 295°C
• Density: 1.313g/cm³
• Vapor Pressure: 1.78E-14mmHg at 25°C
• Refractive Index: 1.519
• CAS DataBase Reference: 3a,6a-dimethyltetrahydroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 3a,6a-dimethyltetrahydroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione(28115-25-5)
• EPA Substance Registry System: 3a,6a-dimethyltetrahydroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione(28115-25-5)

Safety Data

• Hazardous Substances Data: 28115-25-5(Hazardous Substances Data)

Usage

General Description

3a,6a-dimethyltetrahydroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione is a chemical compound with a molecular formula C9H12N4O2. It is a heterocyclic compound with a unique structure, containing both imidazole and imidazolidine rings. 3a,6a-dimethyltetrahydroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione has potential pharmaceutical uses and is being studied for its possible anti-inflammatory and immunomodulatory properties. It has also shown promise in the treatment of cancer, as it has been found to inhibit the growth of certain cancer cells. Additionally, 3a,6a-dimethyltetrahydroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione may also have applications in the field of organic synthesis, serving as a versatile building block in the creation of other complex chemical compounds.

Upstream product

• 807334-29-8 urea phosphate 
• 431-03-8 dimethylglyoxal 
• 135636-66-7 butane-2,3-dione mono-oxime 
• 57-13-6 urea 

Downstream Products

• 89380-44-9 tetrachlorodimethylglycoluril 

Relevant articles and documents

A new and efficient method for the preparation of 2,4,6,8- Tetraazabicyclo[3.3.0]octane-3,7-diones (Glycolurils) catalyzed by keggin, wells-dawson, and preyssler heteropolyoxometalates, effect of structure on the reactivity

Some important cis- and trans-alkyl substituted glycolurils were prepared via condensation of vicinal dicarbonyl compounds with urea and/or methylurea catalyzed by 0.95 mol% of Keggin- type H3PW12O 40 under environmentally benign and simple condition. Proficiency of structurally different heteropolyoxometalates, including Keggin, Wells-Dawson, and Preyssler, was investigated in the reaction of urea with 2, 3-butanedione. A common method was introduced for the isolation of cis- and trans-isomers, role of different solvents was studied, and effect of catalyst mol% was also investigated in this reported.

Synthesis of Glycoluril using Urea Phosphate

Abstract: Glycolurils are building blocks for the synthesis of cucurbiturils that are important host materials for several applications. Glycolurils are prepared conveniently by the condensation of 1,2-diketones with urea using an acid as catalyst. Herein, we report a facile method of synthesis of various glycolurils using urea phosphate and 1,2-diketones.

ACYCLIC CUCURBIT(N)URIL TYPE MOLECULAR CONTAINERS TO TREAT INTOXICATION AND DECREASE RELAPSE RATE IN SUBSTANCE ABUSE DISORDERS

Provided are methods for reversing the effects of drugs of abuse. The method involves administering acyclic CB[n]-type compounds to a mammal in need of the reversal of the effects from a drug of abuse.