Description
Ethyl 1-((tert-butoxycarbonyl)amino)-3,3-difluorocyclobutanecarboxylate (CAS No. 1232365-41-1) is a high-purity fluorinated cyclobutane derivative designed for advanced research and pharmaceutical applications. With the molecular formula C12H19F2NO4, this compound features a unique 3,3-difluorocyclobutane core protected by a tert-butoxycarbonyl (Boc) group, making it an essential intermediate in medicinal chemistry and drug discovery. Its ethyl ester functionality enhances solubility and reactivity, facilitating further synthetic modifications. Ideal for peptide mimetics, enzyme inhibitors, and fluorinated scaffold development, this compound is rigorously tested to meet the highest standards of purity and consistency. Available in various quantities with detailed analytical data (HPLC, NMR, MS) to support your research needs.
Properties
- CAS Number: 1232365-41-1
- Complexity: 368
- IUPAC Name: ethyl 1-(tert-butoxycarbonylamino)-3,3-difluoro-cyclobutanecarboxylate
- InChI: InChI=1S/C12H19F2NO4/c1-5-18-8(16)11(6-12(13,14)7-11)15-9(17)19-10(2,3)4/h5-7H2,1-4H3,(H,15,17)
- InChI Key: OTISFCHOKNSLKD-UHFFFAOYSA-N
- Exact Mass: 279.12821441
- Molecular Formula: C12H19F2NO4
- Molecular Weight: 279.28
- SMILES: CCOC(=O)C1(CC(C1)(F)F)NC(=O)OC(C)(C)C
- Topological: 64.6
- Monoisotopic Mass: 279.12821441
- Synonyms: 1232365-41-1, ethyl 1-((tert-butoxycarbonyl)amino)-3,3-difluorocyclobutanecarboxylate, Cyclobutanecarboxylic acid, 1-[[(1,1-dimethylethoxy)carbonyl]amino]-3,3-difluoro-, ethyl ester, SCHEMBL1967793, DTXSID901134665, ethyl 1-(tert-butoxycarbonylamino)-3,3-difluoro-cyclobutanecarboxylate, DB-084791, Ethyl 1-[[(1,1-dimethylethoxy)carbonyl]amino]-3,3-difluorocyclobutanecarboxylate
Application
Ethyl 1-((tert-butoxycarbonyl)amino)-3,3-difluorocyclobutanecarboxylate is a versatile building block in organic synthesis, particularly for constructing fluorinated cyclobutane scaffolds in drug discovery. It serves as a key intermediate in the development of protease inhibitors, kinase modulators, and other bioactive molecules due to its stereoelectronic properties. The Boc-protected amino group allows for selective deprotection and further functionalization, enabling precise structural diversification. Researchers leverage its rigid, fluorinated core to enhance metabolic stability and binding affinity in target compounds.
If you are interested or have any questions, please contact us at support@atomfair.com
Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


Reviews
There are no reviews yet.