4-Morpholinoaniline
Names
[ CAS No. ]:
2524-67-6
[ Name ]:
4-Morpholinoaniline
[Synonym ]:
benzenamine, 4-(4-morpholinyl)-
4-Morpholinyl aniline
4-Morpholin-4-yl-phenylamine
4-(4-Morpholinyl)aniline
4-(4-Aminophenyl)morpholine
EINECS 219-760-1
Morpholine, 4-(p-aminophenyl)-
4-(morpholin-4-yl)aniline
4-Morpholinoaniline
Benzenamine, 4- (4-morpholinyl)-
4-(Morpholin-4-yl)anilin
p-Morpholinoaniline
4-morpholinobenzenamine
MFCD00006169
Biological Activity
[Description]:
[Related Catalog]:
Chemical & Physical Properties
[ Density]:
1.1±0.1 g/cm3
[ Boiling Point ]:
368.0±37.0 °C at 760 mmHg
[ Melting Point ]:
132-135 °C(lit.)
[ Molecular Formula ]:
C10H14N2O
[ Molecular Weight ]:
178.23
[ Flash Point ]:
176.4±26.5 °C
[ Exact Mass ]:
178.110611
[ PSA ]:
38.49000
[ LogP ]:
0.08
[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C
[ Index of Refraction ]:
1.590
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xn:Harmful;
[ Risk Phrases ]:
R20/21/22
[ Safety Phrases ]:
S26-S37/39-S36/37/39-S22
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2934999090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2934999090
[ Summary ]:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Articles
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 117 , 87-94, (2014)
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 magn...
Electrochemical method for the synthesis of disulfides of 2-(benzo[d]thiazol(or oxazol)-2-ylamino)-5-morpholinobenzenethiol.J. Org. Chem. 78(10) , 5018-21, (2013)
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 o...
Synthesis of novel quinolone and quinoline-2-carboxylic acid (4-morpholin-4-yl-phenyl)amides: a late-stage diversification approach to potent 5HT1B antagonists.Bioorg. Med. Chem. 15(2) , 939-50, (2007)
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-car...