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6345-19-3

3,5,5-Trimethylimidazolidine-2,4-dione

Catalog#: AR00F4HA  |   CAS#: 6345-19-3  |   MDL#: MFCD00152935  |   MF: C6H10N2O2  |   MW: 142.1558

Packsize Purity Price Availability Quantity
100mg 97% $63.00 Global Stock Buy Now Add To Cart
250mg 97% $107.00 Global Stock Buy Now Add To Cart
1g 97% $234.00 Global Stock Buy Now Add To Cart
5g 97% $701.00 Global Stock Buy Now Add To Cart
10g 97% $1,226.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00F4HA
Chemical Name 3,5,5-Trimethylimidazolidine-2,4-dione
CAS Number 6345-19-3
Molecular Formula C6H10N2O2
Molecular Weight 142.1558
MDL Number MFCD00152935
SMILES O=C1NC(C(=O)N1C)(C)C
NSC Number 41220

3,5,5-Trimethylimidazolidine-2,4-dione, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique molecular structure allows for various applications in organic chemistry. When used in chemical synthesis, $name$ serves as a key intermediate in the formation of complex molecules.In organic synthesis, $name$ is utilized as a masked form of amidine functionality. By selectively deprotecting the molecule under specific reaction conditions, chemists can unveil the amidine group, enabling further functionalization. This property makes $name$ a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.Additionally, the presence of the imidazolidine ring in $name$ provides opportunities for the chiral resolution of compounds. Through appropriate derivatization and strategic manipulation of the molecule, enantiomerically pure products can be obtained. This capability is particularly important in drug discovery and development, where enantiomeric purity is often essential for biological activity.Furthermore, 3,5,5-Trimethylimidazolidine-2,4-dione exhibits excellent stability and compatibility with a wide range of reagents and reaction conditions, making it a valuable asset in synthetic organic chemistry. Its ease of manipulation and diverse reactivity make it a highly sought-after compound in the field of chemical synthesis.
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