Interesting facts
Interesting Facts About 1,3-bis(hydroxymethyl)imidazolidin-2-one
1,3-bis(hydroxymethyl)imidazolidin-2-one, often abbreviated as BHI, is a fascinating compound with a variety of applications and properties that capture the interest of scientists and chemistry enthusiasts alike. Here are some intriguing facts:
- Structural Uniqueness: The compound features a five-membered ring structure containing both nitrogen and carbon atoms, which is characteristic of imidazolidines. This unique structure lends to its diverse chemical reactivity.
- Biological Relevance: BHI is significant in biological systems as it can act as a chiral auxiliary in drug synthesis, which is crucial in the creation of enantiomerically pure pharmaceuticals.
- Versatile Building Block: BHI serves as an important intermediate in organic synthesis. Its hydroxymethyl groups provide functional sites that can be modified, leading to a variety of derivatives beneficial in many fields, including medicinal chemistry and materials science.
- Stability and Reactivity: The compound is known for its stability under various conditions while still being reactive enough to participate in important chemical transformations. This balance makes it a valuable asset in synthetic chemistry.
- Potential Applications: Research into BHI has indicated potential uses in areas such as:
- As a polymer additive
- In the development of agrochemicals
- In the formulation of coatings and adhesives
- Environmental Impact: Compounds like BHI are of interest not only for their industrial applications but also for their potential environmental benefits. They may be involved in eco-friendly processes, reducing the reliance on toxic reagents.
In summary, 1,3-bis(hydroxymethyl)imidazolidin-2-one is not just another chemical compound; it represents a convergence of biological relevance, practical applications, and the innovative spirit of modern chemistry. Its continued study may yield exciting discoveries!
Synonyms
136-84-5
1,3-Bis(hydroxymethyl)imidazolidin-2-one
2-Imidazolidinone, 1,3-bis(hydroxymethyl)-
Dimethylol ethylene urea
Carbamol TsEM
Cassurit RI
1,3-Dimethylol-2-imidazolidinone
Zeset S
Dimethylolethyleneurea
Fixapret AH
Karbamol TsEM
Kurbamol TsEM
Quecodur AE
Silesian EM
Verapret AN
Calaroc EU
Neuperm ON
Prym E
Rhonite R 1
1,3-Dimethylolethyleneurea
Cyclic dimethylolethyleneurea
N,N'-Dimethylolethyleneurea
Aerotex Reactant No. 100
Dimethylol cyclic ethyleneurea
Dimethylolcycloethyleneurea
1,3-Bis(hydroxymethyl)-2-imidazolidinone
1,3-Dihydroxymethyl-2-imidazolidone
N,N'-Bis(hydroxymethyl)ethyleneurea
BT 324
N,N'-Dimethylol-N,N'-ethyleneurea
EINECS 205-264-2
NSC 57546
CV678N9PLY
DTXSID5059666
NSC57546
NSC-57546
1,3-Bis(hydroxymethyl)-2-imidazolidone
2-Imidazolidinone,1,3-bis(hydroxymethyl)-
UNII-CV678N9PLY
SCHEMBL133648
DTXCID5034353
AKOS006272946
2-Imidazolidinone,3-bis(hydroxymethyl)-
DB-225909
NS00020473
G82071
Solubility of 1,3-bis(hydroxymethyl)imidazolidin-2-one
1,3-bis(hydroxymethyl)imidazolidin-2-one, with its unique chemical structure, showcases an intriguing solubility profile. This compound is classified as a polar molecule due to the presence of hydroxymethyl groups, which significantly influence its interaction with solvents.
Key Points on Solubility:
In conclusion, the solubility of 1,3-bis(hydroxymethyl)imidazolidin-2-one is predominantly influenced by its polar characteristics, making it well-suited for aqueous environments and certain polar organic solvents. Understanding these solubility properties is essential for its applications in various chemical and pharmaceutical contexts.