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Dioxolane

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Identification
Molecular formula
C4H8O2
CAS number
646-06-0
IUPAC name
1,3-dimethylimidazolidin-2-one
State
State

At room temperature, dioxolane is in a liquid state.

Melting point (Celsius)
-95.20
Melting point (Kelvin)
178.00
Boiling point (Celsius)
78.50
Boiling point (Kelvin)
351.65
General information
Molecular weight
88.11g/mol
Molar mass
88.1060g/mol
Density
1.0770g/cm3
Appearence

Dioxolane is a colorless liquid, and it is known for its sweet ether-like odor.

Comment on solubility

Solubility of 1,3-Dimethylimidazolidin-2-one

1,3-Dimethylimidazolidin-2-one (often abbreviated as DMI) is known for its interesting solubility characteristics. Understanding the solubility of this compound is essential for various applications, especially in the field of organic synthesis and pharmaceutical formulations.

Key Solubility Features

  • Solvent Compatibility: DMI is highly soluble in polar solvents such as water, methanol, and ethanol. Its structure, featuring polar functional groups, contributes to its affinity for these solvents.
  • Hydrogen Bonding: The presence of nitrogen atoms in the imidazolidinone ring allows for extensive hydrogen bonding interactions, which enhances solubility in polar environments.
  • Temperature Dependency: Like many organic compounds, the solubility of DMI may increase with temperature, making it more effective in warmer solutions.
  • Non-Polar Solvents: In contrast, DMI is poorly soluble in non-polar solvents such as hexane or benzene, reflecting its polar nature.

In summary, the solubility properties of 1,3-dimethylimidazolidin-2-one can be summarized as:

  1. Highly soluble in polar solvents.
  2. Good hydrogen bonding capacity.
  3. Temperature-dependent solubility.
  4. Poor solubility in non-polar solvents.

Overall, the solubility of DMI opens up numerous possibilities for its utilization in various chemical reactions and processes, reinforcing its significance in the chemistry landscape.

Interesting facts

Interesting Facts about 1,3-Dimethylimidazolidin-2-one

1,3-Dimethylimidazolidin-2-one is an intriguing compound with various applications and characteristics that make it stand out in the field of chemistry. Here are some fascinating insights about this compound:

  • Structural Significance: It belongs to the family of imidazolidinones, which are cyclic compounds containing nitrogen atoms. The unique structure contributes to its chemical properties and reactivity.
  • Solvent Properties: This compound is often utilized as a solvent in organic chemistry. Its polar nature allows it to dissolve a wide range of substances, making it a valuable tool for scientists.
  • Role in Synthesis: 1,3-Dimethylimidazolidin-2-one is commonly used in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. Its role as a carbamate formation reagent makes it particularly useful.
  • Biological Activity: Research has revealed that this compound exhibits notable biological activities, including anticancer properties. This aspect makes it a subject of interest for medicinal chemistry.
  • Versatile Applications: Beyond its use in organic synthesis, this compound also finds applications in the fields of polymer science and materials chemistry, emphasizing its versatility.

To quote Robert H. Grubbs, a Nobel Laureate in Chemistry, "The beauty of chemistry lies in its ability to transform simple elements into complex molecules with significant properties." 1,3-Dimethylimidazolidin-2-one exemplifies this transformation and opens up avenues for further exploration and innovation in both scientific research and practical applications.

As we delve deeper into its functionalities, the potential for new discoveries and applications continues to evolve, making this compound a captivating subject for chemists and students alike.

Synonyms
1,3-Dimethyl-2-imidazolidinone
80-73-9
1,3-Dimethylimidazolidin-2-one
Dimethyl imidazolidinone
N,N'-Dimethylethyleneurea
1,3-Dimethylimidazolidone
Rhonite 1
DMEU
Karbomos TsEM
2-IMIDAZOLIDINONE, 1,3-DIMETHYL-
N,N'-Dimethylimidazolidinone
Dimethylethyleneurea
1,3-Dimethylethyleneurea
N,N'-Dimethylimidazolidone
1,3-Dimethylimidazolidinone
1,3-Dimethyl-2-imidazolidone
EINECS 201-304-8
UNII-5C1YQQ9M90
MFCD00003188
BRN 0108808
1,3-dimethyl-2-imidazolidinon
NIKKOL DMI
EC 201-304-8
5C1YQQ9M90
DTXSID1073153
N,N'-Dimethyl-2-imidazolidinone
1,3-Dimethyl-imidazolidin-2-one
5-24-01-00054 (Beilstein Handbook Reference)
2-IMIDAZOLIDONE,1,3-DIMETHYL
1,3-DIMETHYL-2-IMIDAZOLIDINONE [MI]
N,N-DIMETHYLETHYLENEDIAMINE CYCLIC UREA
dimethylimidazolidinone
dimethylimidazolidone
SCHEMBL3043
1,3-dimethyl-imidazolidinone
CHEMBL12338
1,3-dimethyl2-imidazolidinone
1,3-dimethylimidazolin-2-one
1,3-dimetyl-2-imidazolidinone
1,3-dimethyl-2-imidazolidone-
1,3-dimethyl-imidazolin-2-one
N,N'-dimethylimidazoline-2-one
1,3-dimethyl 2-imidazolidinone
1,3-dimethyl-2-imadazolidinone
1.3-dimethyl-2-imidazolidinone
1,3-dimethylimidazolidine-2-one
1,3-di-methyl-2-imidazolidinone
1,3-dimethyl imidazolidin-2-one
1,3-dimethyl-2- imidazolidinone
CHEBI:193015
HMS1775L21
STR04040
AKOS001025634
CS-W008767
DIMETHYL IMIDAZOLIDINONE [INCI]
FD49699
PS-3257
1,3-dimethyl-2-imidazolidinone (DMI)
D1477
NS00000061
EN300-60599
1,3-Dimethyl-2-imidazolidinone, reagent grade
D77693
1,3-Dimethyl-2-imidazolidinone, >=99.0% (GC)
Q2463110
Z56755571
F0001-2089
N,N'-Dimethyl-ethylene-urea;1,3-Dimethylimidazolidin-2-one
1,3-Dimethyl-2-imidazolidinone, absolute, over molecular sieve (H2O <=0.04%), >=99.5% (GC)
1,3-dimethyl-2-imidazolidinone;1,3-dimethylimidazolidin-2-one;2-imidazolidinone, 1,3-dimethyl-;1,3-dimethyl-2-imidazolidinone 1,3-dimethylimidazolidin-2-one 2-imidazolidinone, 1,3-dimethyl-