| Identification | More | [Name]
4-(4-NITROPHENYL)MORPHOLINE | [CAS]
10389-51-2 | [Synonyms]
4-(4-NITROPHENYL)MORPHOLINE
4-MORPHOLINO NITRO BENZENE
4-(P-NITROPHENYL)MORPHOLINE
AURORA 1260
BUTTPARK 97\12-12
N-(4-NITROPHENYL)MORPHOLINE
TIMTEC-BB SBB006371
4-(4-nitrophenyl)-morpholin
4-(p-nitrophenyl)-morpholin
4-Morpholino-1-nitrobenzene
p-Morpholinonitrobenzene | [EINECS(EC#)]
233-851-3 | [Molecular Formula]
C10H12N2O3 | [MDL Number]
MFCD00023317 | [Molecular Weight]
208.21 | [MOL File]
10389-51-2.mol |
| Chemical Properties | Back Directory | [Melting point ]
152 °C | [Boiling point ]
386.2±37.0 °C(Predicted) | [density ]
1.265±0.06 g/cm3(Predicted) | [RTECS ]
QE7405000 | [storage temp. ]
Storage temp. 2-8°C | [solubility ]
soluble in Dimethylformamide | [form ]
powder to crystal | [pka]
0.81±0.40(Predicted) | [color ]
Light yellow to Yellow to Orange | [λmax]
375nm(Dioxane)(lit.) | [InChI]
InChI=1S/C10H12N2O3/c13-12(14)10-3-1-9(2-4-10)11-5-7-15-8-6-11/h1-4H,5-8H2 | [InChIKey]
IAJDSUYFELYZCS-UHFFFAOYSA-N | [SMILES]
N1(C2=CC=C([N+]([O-])=O)C=C2)CCOCC1 | [CAS DataBase Reference]
10389-51-2(CAS DataBase Reference) | [EPA Substance Registry System]
Morpholine, 4-(4-nitrophenyl)- (10389-51-2) |
| Safety Data | Back Directory | [Risk Statements ]
R40:Limited evidence of a carcinogenic effect.
R42/43:May cause sensitization by inhalation and skin contact .
R63:Possible risk of harm to the unborn child. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [RIDADR ]
1662 | [TSCA ]
Yes | [HS Code ]
2934999090 |
| Hazard Information | Back Directory | [Synthesis Reference(s)]
Synthesis, p. 1145, 1990 DOI: 10.1055/s-1990-27118 | [Synthesis]
GENERAL METHODS: Aryl halides (1.0 mmol), morpholine (1 mmol), sodium tert-butoxide (2 mmol) and 0.2 mol% of Pd/Nf-G catalyst were sequentially added to 1 mL of dimethyl sulfoxide (DMSO). The reaction mixture was stirred at 110 °C for 12 h. The reaction process was monitored by gas chromatography (GC). Upon completion of the reaction, the mixture was cooled to room temperature and extracted with ethyl acetate. The catalyst was recovered by simple filtration and subsequently washed with ethanol, dried and stored for subsequent use. The crude product was purified by column chromatography with the eluent being a mixed petroleum ether/ethyl acetate solvent. The recovered catalyst was reused in subsequent recyclability studies. The conversion of the reactants was determined by gas chromatography (GC). | [References]
[1] Bulletin of the Chemical Society of Japan, 1991, vol. 64, # 1, p. 42 - 49
[2] Applied Organometallic Chemistry, 2013, vol. 27, # 12, p. 704 - 706
[3] RSC Advances, 2014, vol. 4, # 96, p. 53387 - 53396
[4] Tetrahedron Letters, 2015, vol. 56, # 30, p. 4463 - 4467
[5] Tetrahedron Letters, 2016, vol. 57, # 14, p. 1532 - 1536 |
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