7529-22-8
Chemical Structure
4-Methylmorpholine N-oxide
Synonym(s): N-Methylmorpholine N-Oxide; MMNO; 4-Methylmorpholine 4-oxide
- CAS No.: 7529-22-8
- Formula:C5H11NO2
- Molecular Weight:117.15
IUPAC Name: 4-methylmorpholine 4-oxide
InChIKey: LFTLOKWAGJYHHR-UHFFFAOYSA-N
SMILES: C[N+]1([O-])CCOCC1
Biological Activity: 4-Methylmorpholine N-oxide (N-Methylmorpholine N-Oxide; MMNO; 4-Methylmorpholine 4-oxide) is an amine oxide ligand and ozonation reagent. 4-Methylmorpholine N-oxide forms coordination complexes with lanthanum (III) nitrate and yttrium (III) nitrate via its nitroso oxygen atom. The metal-ligand bonds are dominated by electrostatic interactions with a small covalent component. 4-Methylmorpholine N-oxide is applicable in ozonation reactions for the synthesis of methyl 9-oxononanoate[1][2].
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4-Methylmorpholine N-oxide | 99.95% | 4-Methylmorpholine N-oxide (N-Methylmorpholine N-Oxide; MMNO; 4-Methylmorpholine 4-oxide) is an amine oxide ligand and ozonation reagent. 4-Methylmorpholine N-oxide forms coordination complexes with lanthanum (III) nitrate and yttrium (III) nitrate via its nitroso oxygen atom. The metal-ligand bonds are dominated by electrostatic interactions with a small covalent component. 4-Methylmorpholine N-oxide is applicable in ozonation reactions for the synthesis of methyl 9-oxononanoate. | ||||||||||||||||||||
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References
- [1]. Wang H, et al. Synthesis of chemically edited derivatives of the endogenous regulator of inflammation 9-PAHSA. J Antibiot (Tokyo). 2019;72(6):498-506. [Content Brief]
- [2]. Bezerra R F, et al. Addition compounds between 4-methylmorpholine-N-oxide (MMNO) and some lanthanides (III) and yttrium (III) nitrates[J]. Journal of alloys and compounds, 2002, 344(1-2): 120-122.
