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N-METHYL-N-(4-NITROBENZYL)AMINE HYDROCHLORIDE

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N-METHYL-N-(4-NITROBENZYL)AMINE HYDROCHLORIDE Basic information

Product Name:
N-METHYL-N-(4-NITROBENZYL)AMINE HYDROCHLORIDE
Synonyms:
  • N-METHYL-4-NITROBENZYLAMINE HYDROCHLORIDE
  • N-METHYL-N-(4-NITROBENZYL)AMINE HYDROCHLORIDE
  • N-Methyl-N-(4-nitrobenzyl)amineHCl
  • 4-Nitro-N-methylbenzylamine
  • N-METHYL-N-(4-NITROBENZYL)AMINE
  • N-METHYL-N-(4-NITROB
  • N-Methyl-4-nitrobenzylaMine
  • Methyl[(4-nitrophenyl)Methyl]aMine hydrochloride
CAS:
19499-60-6
MF:
C8H10N2O2
MW:
166.18
Product Categories:
  • Polyamines
Mol File:
19499-60-6.mol
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N-METHYL-N-(4-NITROBENZYL)AMINE HYDROCHLORIDE Chemical Properties

Melting point:
218 °C
Boiling point:
277.2±15.0 °C(Predicted)
Density 
1.162±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
Solid
pka
8.86±0.10(Predicted)
Appearance
Brown to reddish brown Solid
CAS DataBase Reference
19499-60-6
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Safety Information

Hazard Codes 
Xi
HS Code 
2921490090
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N-METHYL-N-(4-NITROBENZYL)AMINE HYDROCHLORIDE Usage And Synthesis

Synthesis

555-16-8

74-89-5

19499-60-6

GENERAL STEPS: To prepare N-methyl-4-nitrobenzylamine; 4-nitrobenzaldehyde (15.0 g, 99.3 mmol) and 40% aqueous methylamine (17 mL) in methanol (250 mL) were mixed for 15 min at 0 °C, followed by addition of sodium borohydride (3.77 g). The reaction mixture was stirred at room temperature for 2 hours and then concentrated. Water (50 mL) was added to the residue and extracted with dichloromethane (3 x 250 mL). The organic phases were combined, dried and concentrated to give the target product N-methyl-4-nitrobenzylamine. Yield 15.4 g, 94% yield.1H NMR (CDCl3) δ 8.10 (m, 2H), 7.43 (m, 2H), 3.79 (s, 2H), 2.39 (s, 3H).MS (AP+) m/e 167 (MH+).

References

[1] Patent: WO2008/4117, 2008, A1. Location in patent: Page/Page column 116
[2] Molecules, 2017, vol. 22, # 12,

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