Diethyl 1,3-acetonedicarboxylate CAS: 105-50-0
Catalog Number | XD93860 |
Product Name | Diethyl 1,3-acetonedicarboxylate |
CAS | 105-50-0 |
Molecular Formula | C9H14O5 |
Molecular Weight | 202.2 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
Diethyl 1,3-acetonedicarboxylate is a chemical compound with a molecular formula C10H16O4. This compound is commonly used as a reagent in organic chemistry reactions. It serves as a versatile building block for the synthesis of various compounds due to its unique chemical properties.One of the primary uses of diethyl 1,3-acetonedicarboxylate is in the formation of heterocyclic compounds. It can readily undergo condensation reactions with various nucleophiles and electrophiles to form a wide range of heterocycles, such as pyridines, pyrimidines, and pyrazines. These heterocyclic compounds are valuable in the development of pharmaceuticals, agrochemicals, and other industrial chemicals.Additionally, diethyl 1,3-acetonedicarboxylate is commonly employed in the synthesis of natural products and medicinally important compounds. It can act as a building block for the introduction of functional groups, such as esters, ketones, and carboxylic acids, into organic molecules. By incorporating these functional groups into target compounds, researchers can modify their properties, such as solubility, stability, and biological activity.Furthermore, diethyl 1,3-acetonedicarboxylate has been utilized in the synthesis of chiral compounds. It can undergo asymmetric reactions, allowing the production of optically active compounds, which are essential in pharmaceuticals and fine chemical synthesis. These asymmetric reactions are achieved by using chiral catalysts or employing resolution techniques to separate enantiomers.Another important application of diethyl 1,3-acetonedicarboxylate is its use as a starting material for the synthesis of flavor and fragrance compounds. By reacting with suitable reagents or functional groups, it can be transformed into compounds with pleasant aromas or flavors, which are widely utilized in the food, cosmetics, and perfumery industries.It is crucial to handle diethyl 1,3-acetonedicarboxylate with care as it is flammable and can cause irritation to the skin, eyes, and respiratory system. Proper safety precautions, such as wearing protective clothing and working in a well-ventilated area, should be followed when using this compound.In conclusion, diethyl 1,3-acetonedicarboxylate is a versatile compound extensively used in organic synthesis. Its ability to form heterocycles, serve as a building block for functional groups, and enable asymmetric reactions make it an important reagent in the development of various compounds, including pharmaceuticals, agrochemicals, flavors, and fragrances. However, caution must be exercised when handling this compound to ensure personal safety.