126527
2,6-Dimethylmorpholine
97%
Synonym(s):
2,6-Dimethylmorpholine
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About This Item
Empirical Formula (Hill Notation):
C6H13NO
CAS Number:
Molecular Weight:
115.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-509-3
Beilstein/REAXYS Number:
103036
MDL number:
Assay:
97%
InChI
1S/C6H13NO/c1-5-3-7-4-6(2)8-5/h5-7H,3-4H2,1-2H3
InChI key
HNVIQLPOGUDBSU-UHFFFAOYSA-N
SMILES string
CC1CNCC(C)O1
assay
97%
refractive index
n20/D 1.446 (lit.)
bp
147 °C (lit.)
mp
−85 °C (lit.)
density
0.935 g/mL at 25 °C (lit.)
functional group
ether
Quality Level
Application
cis-2,6-Dimethylmorpholine (DMMP) has been used in the preparation of microporous material composed of hybrid T2 and T3 supertetrahedral clusters.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Flam. Liq. 3 - Skin Corr. 1B
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
118.4 °F - closed cup
flash_point_c
48 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Xiaohui Han et al.
Chemical communications (Cambridge, England), 50(7), 796-798 (2013-12-03)
Solvothermal reactions of S, Ga and Sn using cis-2,6-dimethylmorpholine (DMMP) as an organic template, in the presence of a trace amount of H2O at 180 °C, generated microporous [C6H14NO]14.4[Ga6.40Sn21.60S52O8] material composed of hybrid T2 and T3 supertetrahedral clusters with a
S S Mirvish et al.
Cancer research, 43(6), 2550-2554 (1983-06-01)
We reported previously that mice exposed to atmospheric NO2 contained a nitrosating agent (NSA) that reacted with morpholine in aqueous methanol homogenates of the mice to give N-nitrosomorpholine. We have now found that N-nitrosomorpholine was also produced by reacting morpholine
Natalia Szkaradek et al.
Anti-cancer agents in medicinal chemistry, 19(16), 1949-1965 (2019-04-06)
Natural plant metabolites and their semisynthetic derivatives have been used for years in cancer therapy. Xanthones are oxygenated heterocyclic compounds produced as secondary metabolites by higher plants, fungi or lichens. Xanthone core may serve as a template in the synthesis
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