254454-54-1
254454-54-1
Chemical Structure
1-Boc-3-iodoazetidine
- CAS No.: 254454-54-1
- Formula:C8H14INO2
- Molecular Weight:283.11
IUPAC Name: tert-butyl 3-iodoazetidine-1-carboxylate
InChIKey: XPDIKRMPZNLBAC-UHFFFAOYSA-N
SMILES: O=C(N1CC(C1)I)OC(C)(C)C
Biological Activity: 1-Boc-3-iodoazetidine acts as a bifunctional additive for lithium-oxygen (Li-O2) batteries and can be used to enhance the performance of Li-O2 batteries. 1-Boc-3-iodoazetidine is applied in the synthesis of C3-functionalized azetidines and C2-functionalized azetidines via a lithium/iodine exchange or β-elimination/lithiation reaction sequence[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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1-Boc-3-iodoazetidine | 98.97% | 1-Boc-3-iodoazetidine acts as a bifunctional additive for lithium-oxygen (Li-O2) batteries and can be used to enhance the performance of Li-O2 batteries. 1-Boc-3-iodoazetidine is applied in the synthesis of C3-functionalized azetidines and C2-functionalized azetidines via a lithium/iodine exchange or β-elimination/lithiation reaction sequence. | ||||||||||||||||||||
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References
- [1]. Li YN, et al. Bifunctional 1-Boc-3-Iodoazetidine Enhancing Lithium Anode Stability and Rechargeability of Lithium-Oxygen Batteries. ACS Appl Mater Interfaces. 2021;13(14):16437-16444. [Content Brief]
- [2]. Colella M, et al. Development of a Continuous Flow Synthesis of 2-Substituted Azetines and 3-Substituted Azetidines by Using a Common Synthetic Precursor. J Org Chem. 2021;86(20):13943-13954. [Content Brief]
