4-(Morpholinomethyl)aniline

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Products Intro: CAS:51013-67-3
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CAS:51013-67-3
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CAS:51013-67-3
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4-(Morpholinomethyl)aniline manufacturers

4-(Morpholinomethyl)aniline Basic information
Product Name:4-(Morpholinomethyl)aniline
Synonyms:BUTTPARK 98\57-95;CHEMBRDG-BB 4011238;ASISCHEM U94603;AKOS MSC-0181;AKOS BBS-00006785;4-(MORPHOLINOMETHYL)ANILINE;4-(MORPHOLIN-4-YLMETHYL)ANILINE;4-MORPHOLIN-4-YLMETHYL-PHENYLAMINE
CAS:51013-67-3
MF:C11H16N2O
MW:192.26
EINECS:
Product Categories:Benzene series;Amines;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:51013-67-3.mol
4-(Morpholinomethyl)aniline Structure
4-(Morpholinomethyl)aniline Chemical Properties
Melting point 95-97°C
Boiling point 320.7±27.0 °C(Predicted)
density 1.136±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka7.26±0.10(Predicted)
AppearanceWhite to light yellow Solid
CAS DataBase Reference51013-67-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,C
Risk Statements 20/21/22-34
Safety Statements 26-36/37/39-45-22
HazardClass IRRITANT
HS Code 2934999090
MSDS Information
4-(Morpholinomethyl)aniline Usage And Synthesis
Uses4-(Morpholinomethyl)aniline is an aniline derivative used in the preparation of tyrosine kinase inhibitors.
Synthesis
4-(4-NITROBENZYL)MORPHOLINE

6425-46-3

4-(Morpholinomethyl)aniline

51013-67-3

General procedure for the synthesis of 4-morpholinomethylaniline from 4-(4-nitrobenzyl)morpholine: 4-(4-nitrobenzyl)morpholine (2.22 g, 10 mmol) was dissolved in methanol under nitrogen atmosphere and 200 mg of Pd/C catalyst was added. Hydrogen was then passed through to carry out the hydrogenation reaction, which lasted for 6 hours. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was collected. The filtrate was concentrated to give 1.83 g of 4-morpholinomethylaniline solid in 95% yield.

References[1] Journal of Medicinal Chemistry, 2008, vol. 51, # 12, p. 3507 - 3525
[2] RSC Advances, 2015, vol. 5, # 58, p. 47125 - 47130
[3] Patent: CN106432235, 2017, A. Location in patent: Paragraph 0091; 0092
[4] Organic Process Research and Development, 2006, vol. 10, # 3, p. 493 - 499
[5] Journal of Medicinal Chemistry, 2018, vol. 61, # 4, p. 1499 - 1518
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