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54300-20-8

4-ethyl-1,3-oxazole

Catalog#: AR01B7HQ  |   CAS#: 54300-20-8  |   MDL#: MFCD16249872  |   MF: C5H7NO  |   MW: 97.1152

Packsize Purity Price Availability Quantity
250mg 95% $419.00 2-3 weeks Buy Now Add To Cart
500mg 95% $644.00 2-3 weeks Buy Now Add To Cart
1g 95% $819.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $1,693.00 2-3 weeks Buy Now Add To Cart
5g 95% $3,321.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR01B7HQ
Chemical Name 4-ethyl-1,3-oxazole
CAS Number 54300-20-8
Molecular Formula C5H7NO
Molecular Weight 97.1152
MDL Number MFCD16249872
SMILES CCc1cocn1

4-Ethyl-1,3-oxazole is a versatile building block in chemical synthesis due to its unique structure and reactivity. This compound has found widespread application in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of various biologically active compounds. Its heterocyclic structure imparts distinct properties that make it highly valuable in organic chemistry.One of the key applications of 4-Ethyl-1,3-oxazole is in the synthesis of heterocyclic scaffolds, which are prevalent in many drug molecules. By incorporating this moiety into a molecule, chemists can introduce specific functionalities or spatial arrangements that enhance the biological activity or pharmacokinetic properties of the final compound. Additionally, 4-Ethyl-1,3-oxazole can serve as a precursor for the formation of other heterocycles through cyclization reactions, allowing for the efficient construction of complex molecular frameworks.Furthermore, 4-Ethyl-1,3-oxazole can participate in various functionalization reactions, enabling the introduction of different substituents or modifications at specific positions on the oxazole ring. This flexibility makes it a valuable building block for the diversification of chemical libraries for drug discovery and development. The synthetic accessibility and versatility of 4-Ethyl-1,3-oxazole make it a valuable tool for organic chemists seeking to design and synthesize novel compounds with potential biological activities.
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