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Formule empirique (notation de Hill) :
C5H11NO2
Numéro CAS:
Poids moléculaire :
117.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Form:
liquid
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Laissez-nous vous aiderInChI
1S/C5H11NO2/c1-6(7)2-4-8-5-3-6/h2-5H2,1H3
SMILES string
C[N+]1([O-])CCOCC1
InChI key
LFTLOKWAGJYHHR-UHFFFAOYSA-N
form
liquid
reaction suitability
reagent type: oxidant
concentration
50 wt. % in H2O
refractive index
n20/D 1.4201
pH
9.00 ( in neat)
bp
118.5 °C
mp
−20 °C
density
1.13 g/mL at 25 °C
functional group
ether
storage temp.
2-8°C
Quality Level
Catégories apparentées
Application
Oxidant for synthesis of novel organic polymer - inorganic hybrid for use as a catalyst for asymmetrical epoxidation
Reagent or Reactant for:
Used as a pretreatment for techno-economical study of ethanol and biogas production from spruce wood
Reagent or Reactant for:
- Cyclocondensation and cyclization in the enantioselective synthesis of oxazolomycin A
- Wharton rearrangement and stereoselective dihydroxylation reactions
- Reduction of amine N-oxides by diboron reagents
- Synthesis of polysaccharide blend fibers
- Synthesis of cellulose / modified nano-SiO2 composite packaging films
- Copper-catalyzed oxidative coupling for preparation of propargylamines
Used as a pretreatment for techno-economical study of ethanol and biogas production from spruce wood
- 4-Methylmorpholine N-oxide (NMO) is widely used as a co-oxidant to regenerate osmium tetroxide (OsO4) catalyst during dihydroxylation of alkenes.
- In the presence of catalytic amounts of tetra-n-propylammonium perruthenate (TPAP), NMO oxidizes secondary amines to the corresponding imines.
- 4-Methylmorpholine N-oxide solution can be used to oxidize activated primary halides to aldehydes and secondary halides to ketones, respectively.
- It can also be used to promote stereoselective intermolecular Pauson-Khand reaction for the synthesis of cyclopentenones.
signalword
Warning
hcodes
Hazard Classifications
Repr. 2
Classe de stockage
10 - Combustible liquids
wgk
WGK 1
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Catalytic Osmium Tetroxide Oxidation of Olefins: cis?1, 2?Cyclohexanediol.
VanRheenen V, et al.
Organic Syntheses, 43-43 (1988)
Oxidation of activated halides to aldehydes and ketones by N-methylmorpholine-N-oxide.
Griffith W P, et al.
Synthetic Communications, 22(13), 1967-1971 (1992)
Asymmetric dihydroxylation via ligand-accelerated catalysis.
Jacobsen E N, et al.
Journal of the American Chemical Society, 110(6), 1968-1970 (1988)
Catalytic oxidation of secondary amines with tetra-n-propylammonium perruthenate.
Goti A and Romani M
Tetrahedron Letters, 35(35), 6567-6570 (1994)
Qiang Li et al.
Bioresource technology, 107, 251-257 (2012-01-10)
To fully exploit the benefits of N-methylmorpholine-N-oxide (NMMO) in lignocelluloses bioconversion, a compatible system was established for efficient in situ saccharification of cellulose in NMMO-aqueous media in which the NMMO is able to activate and solubilize the cellulose, and the
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