AE25725
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 97% | in stock | $49.00 | $35.00 | - + | |
250mg | 97% | in stock | $80.00 | $56.00 | - + | |
1g | 97% | in stock | $210.00 | $147.00 | - + | |
5g | 97% | in stock | $768.00 | $538.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE25725 |
Chemical Name: | Ethyl 2-(oxetan-3-yl)acetate |
CAS Number: | 1207175-04-9 |
Molecular Formula: | C7H12O3 |
Molecular Weight: | 144.1684 |
MDL Number: | MFCD14586417 |
SMILES: | CCOC(=O)CC1COC1 |
Complexity: | 118 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 3 |
Rotatable Bond Count: | 4 |
XLogP3: | 0.3 |
Ethyl 2-(oxetan-3-yl)acetate is a valuable compound in chemical synthesis, particularly in the field of organic chemistry. This versatile compound is widely used as a building block in the synthesis of complex molecules and pharmaceutical intermediates. Its unique structure containing a fused oxetane ring makes it a valuable precursor in the development of various pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, Ethyl 2-(oxetan-3-yl)acetate can serve as a key starting material for the construction of more elaborate molecules through various synthetic pathways. Its oxetane ring provides a reactive site for selective functionalization, allowing chemists to introduce specific substituents or structural motifs. This compound is often employed in the synthesis of bioactive compounds, natural products, and fine chemicals where the oxetane ring can impart desirable properties or pharmacological activities.Furthermore, the presence of both an ester and an oxetane group in Ethyl 2-(oxetan-3-yl)acetate offers diverse reactivity and synthetic possibilities. The ester functionality can be readily manipulated to introduce other functional groups or participate in cascade reactions, while the oxetane ring can undergo ring-opening reactions to access a variety of derivatives with controlled stereochemistry.Overall, Ethyl 2-(oxetan-3-yl)acetate is a valuable tool in the hands of synthetic chemists for the efficient and selective construction of complex molecules with potential applications in drug discovery, material science, and other chemical industries.