| Chemical Name: | methyl 3-(hydroxymethyl)oxetane-3-carboxylate |
| CAS Number: | 1780733-73-4 |
| Product Number: | AG01JV8U(AGN-PC-3H6MOO) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | |
| Molecular Weight: |
Methyl 3-(hydroxymethyl)oxetane-3-carboxylate, commonly known as $name$, serves as a versatile building block in chemical synthesis due to its unique structure and reactivity. This compound plays a crucial role in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals through its involvement in key synthetic pathways.In organic synthesis, $name$ can undergo functional group transformations to introduce a hydroxymethyl group and an oxetane moiety into target molecules. The hydroxymethyl group offers opportunities for further derivatization, enabling the introduction of various functional groups to tailor the properties of the final product. Additionally, the oxetane ring structure contributes to the molecular rigidity and conformational control of the synthesized compounds.Furthermore, the presence of the carboxylate group in $name$ facilitates its use as a protecting group in organic chemistry reactions. By selectively masking reactive functional groups in a molecule, the carboxylate moiety helps to direct the regioselective and stereoselective synthesis of complex organic compounds.Overall, the application of Methyl 3-(hydroxymethyl)oxetane-3-carboxylate in chemical synthesis offers a powerful tool for designing and constructing structurally diverse and functionally rich molecules with potential applications in various industries.
![O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]](https://img.angenechemical.com/storage/3a59/3a5932eec850ab245f6f4d4a7f9497f9.png)
(Cl)Cl)c1c(C)cc(cc1C)C](https://img.angenechemical.com/storage/6693/66939a3f08a27d2b6717c3194e00970b.png)
