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METHYL 3-METHYLAMINOCROTONATE

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METHYL 3-METHYLAMINOCROTONATE Basic information

Product Name:
METHYL 3-METHYLAMINOCROTONATE
Synonyms:
  • METHYL 3-(METHYLAMINO)BUT-2-ENOATE
  • METHYL 3-METHYLAMINOCROTONATE
  • Methyl 3-methylaminocrotonate,97%
  • Methyl beta-(methylamino)crotonate
  • 2-Butenoic acid, 3-(MethylaMino)-, Methyl ester
  • 3-Methylaminobut-2-enoic acid methyl ester
  • Methyl 3-(methylamino)-2-butenoate
  • beta-N-methylaminocapronic acid methyl ester
CAS:
13412-12-9
MF:
C6H11NO2
MW:
129.16
Mol File:
13412-12-9.mol
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METHYL 3-METHYLAMINOCROTONATE Chemical Properties

Melting point:
62-68 °C
Boiling point:
187.5±23.0 °C(Predicted)
Density 
0.969±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
solid
pka
5.73±0.70(Predicted)
Appearance
White to off-white Solid
Water Solubility 
Soluble in water at (54 g/L) (25°C), Calc.
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26
HS Code 
29224985

MSDS

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
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METHYL 3-METHYLAMINOCROTONATE Usage And Synthesis

Chemical Properties

white crystalline powder

Uses

It is employed as an intermediate in the synthesis of an analogue to amlodipine, bearing a short amino polyethylene glycol chain.

Synthesis

105-45-3

74-89-5

13412-12-9

1.2 g of silica gel was added to 11.6 g (100 mmol, 1 eq.) of methyl acetoacetate. To this was added 9.25 g (120 mmol, 1.2 eq.) of methylamine solution (40% aqueous solution) and the mixture was stirred overnight. The reaction mixture was extracted with dichloromethane (DCM), dried with anhydrous magnesium sulfate (MgSO?), filtered and the solvent was evaporated to give the yellow oily product methyl 3-(methylamino)but-2-enoate in 12.21 g, 95% yield.1H-NMR (CDCl?, δ/ppm): 8.47 (s, NH, 1H), 4.47 (s, CH, 1H). 3.61 (s, OCH?, 3H), 2.91 (d, NHCH?, J = 5.22 Hz, 3H), 1.92 (s, CH?, 3H).

References

[1] RSC Advances, 2015, vol. 5, # 49, p. 39193 - 39204
[2] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 8, p. 1944 - 1947
[3] Patent: WO2013/25733, 2013, A1. Location in patent: Paragraph 0402
[4] Chemical and Pharmaceutical Bulletin, 1987, vol. 35, # 12, p. 4819 - 4828
[5] Bulletin de la Societe Chimique de France, 1923, vol. <4> 33, p. 1108

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