26272-85-5
26272-85-5
Chemical Structure
3-Iodooxetane
- CAS No.: 26272-85-5
- Formula:C3H5IO
- Molecular Weight:183.98
IUPAC Name: 3-iodooxetane
InChIKey: KBEIFKMKVCDETC-UHFFFAOYSA-N
SMILES: IC1COC1
Biological Activity: 3-Iodooxetane is a synthetic oxetane alkyl iodide reagent used for N-alkylation. 3-Iodooxetane can be used to prepare pyrazolo-oleanolic acid derivatives and serves as an alkyl iodide substrate in electrochemical halogen atom transfer alkylation[1][2].
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3-Iodooxetane | 99.95% | 3-Iodooxetane is a synthetic oxetane alkyl iodide reagent used for N-alkylation. 3-Iodooxetane can be used to prepare pyrazolo-oleanolic acid derivatives and serves as an alkyl iodide substrate in electrochemical halogen atom transfer alkylation. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.74
HY-W0049253-Oxetanemethanol -
Similarity Score 0.70
HY-76476R(S)-Tetrahydrofuran-3-ol (Standard) -
Similarity Score 0.67
HY-764403-Oxetanone -
Similarity Score 0.65
HY-Y1010ROxiran-2-ylmethanol (Standard) -
Similarity Score 0.65
HY-W0158634-Chlorotetrahydro-2H-pyran -
Similarity Score 0.63
HY-107931RPropiolactone (Standard) -
Similarity Score 0.63
HY-Z1630RRivaroxaban impurity 6 (Standard) -
Similarity Score 0.62
HY-W013042Cyclobutanol -
Similarity Score 0.62
HY-79631(Tetrahydro-2H-pyran-4-yl)methanol -
Explore the MedChemAI to find more analogs
References
- [1]. Yu Y, et al. Synthesis and biological evaluation of pyrazole-fused oleanolic acid derivatives as novel inhibitors of inflammatory and osteoclast differentiation. Bioorganic & medicinal chemistry. 2023 Feb 15;80:117177. [Content Brief]
- [2]. Sun X, et al. Electrochemical halogen-atom transfer alkylation via α-aminoalkyl radical activation of alkyl iodides. Nature communications. 2023 Oct 26;14(1):6825.
