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About This Item
Empirical Formula (Hill Notation):
C10H14N2O
CAS Number:
Molecular Weight:
178.23
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
assay
≥98%
form
solid
mp
132-135 °C (lit.)
functional group
ether
SMILES string
Nc1ccc(cc1)N2CCOCC2
InChI
1S/C10H14N2O/c11-9-1-3-10(4-2-9)12-5-7-13-8-6-12/h1-4H,5-8,11H2
InChI key
PHNDZBFLOPIMSM-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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A green approach for the electrochemical synthesis of 4-morpholino-2-(arylsulfonyl) benzenamines.
Nematollahi D and Esmaili R.
Tetrahedron Letters, 51(37), 4862-4865 (2010)
Roya Esmaili et al.
The Journal of organic chemistry, 78(10), 5018-5021 (2013-05-01)
Electrochemical synthesis of two new disulfides of 2-(benzo[d]thiazol(or oxazol)-2-ylamino)-5-morpholinobenzene thiols was carried out via the electrooxidation of 4-morpholinoaniline in the presence of 2-mercaptobenzothiazole and 2-mercaptobenzoxazole. Our results indicate that electrogenerated p-quinonediimine participated in a Michael-type addition reaction with 2-SH-benzazoles and
K Dhahagani et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 117, 87-94 (2013-08-30)
Metal(II) chelates of Schiff bases derived from the condensation of 4-morpholinoaniline with substituted salicylaldehyde have been prepared and characterized by (1)H NMR, IR, electronic, EPR, and magnetic measurement studies. The complexes are of the type M(X-MPMP)2 [where M=Cu(II), Co(II)), Zn(II)
Carey L Horchler et al.
Bioorganic & medicinal chemistry, 15(2), 939-950 (2006-11-28)
Multiparallel amenable syntheses of 6-methoxy-8-amino-4-oxo-1,4-dihydroquinoline-2-carboxylic acid-(4-morpholin-4-yl-phenyl)amides (I) and 4-amino-6-methoxy-8-(4-methyl-piperazin-1-yl)-quinoline-2-carboxylic acid (4-morpholin-4-yl-phenyl)amides (II) which facilitate late-stage diversification at the 8-position of (I) and at the 4- and 8-positions of (II) are described. The resulting novel series were determined to contain potent
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