Basic information Safety Supplier Related

3-Amino-3-(3,4-dimethoxyphenyl)propionic acid

Basic information Safety Supplier Related

3-Amino-3-(3,4-dimethoxyphenyl)propionic acid Basic information

Product Name:
3-Amino-3-(3,4-dimethoxyphenyl)propionic acid
Synonyms:
  • 3-AMINO-3-(3 4-DIMETHOXYPHENYL)PROPIONI&
  • 3-Amino-3-(3,4-dimethoxyphenyl)propionic acid
  • 3-Amino-3-(3,4-dimethoxyphenyl)propionic acid, beta-Amino-3,4-dimethoxyhydrocinnamic acid
  • 3-aMino-3-(3,4- diMethoxyphenyl)propionoic acid
  • 3-ammonio-3-(3,4-dimethoxyphenyl)propanoate
  • 3-ammonio-3-(3,4-dimethoxyphenyl)propionate
  • 3-azaniumyl-3-(3,4-dimethoxyphenyl)propanoate
  • 573426_ALDRICH
CAS:
34841-09-3
MF:
C11H15NO4
MW:
225.24
EINECS:
202-110-6
Product Categories:
  • API intermediates
  • C11 to C12
  • Carbonyl Compounds
  • Carboxylic Acids
Mol File:
34841-09-3.mol
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3-Amino-3-(3,4-dimethoxyphenyl)propionic acid Chemical Properties

Melting point:
223 °C (dec.) (lit.)
Boiling point:
379.7±42.0 °C(Predicted)
Density 
1.212±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
powder to crystal
pka
3.73±0.10(Predicted)
color 
White to Almost white
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
HS Code 
29224999
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3-Amino-3-(3,4-dimethoxyphenyl)propionic acid Usage And Synthesis

Synthesis

141-82-2

120-14-9

34840-85-2

3,4-dimethoxybenzaldehyde (50 g, 0.33 mol) and ammonium acetate (50 g) were mixed in 95% ethanol (50 ml). The mixture was heated to 50 °C, followed by slow addition of malonic acid (63 g, 0.6 mol) and supplemented with 95% ethanol (25 ml). The reaction mixture was refluxed for 3 hours and then the reaction was continued at 80°C for 24 hours. Upon completion of the reaction, the precipitate was collected by filtration, washed with ethanol and recrystallized in 50% ethanol to afford 47.8 g of the target product 3-amino-3-(3,4-dimethoxyphenyl)propionic acid as a white solid (yield: 65%). The product was characterized by 1H NMR (300 MHz, D2O): δ 6.90-6.87 (m, 3H), 4.44-4.39 (t, 1H), 3.69 (s, 3H), 3.67 (s, 3H), 2.76-2.57 (m, 2H). Mass spectrum (EI) m/z: 226 (M++H).

References

[1] Chemical Communications, 2011, vol. 47, # 20, p. 5894 - 5896
[2] Patent: WO2010/16939, 2010, A1. Location in patent: Page/Page column 57
[3] Synlett, 2013, vol. 24, # 6, p. 733 - 736
[4] ACS Medicinal Chemistry Letters, 2014, vol. 5, # 11, p. 1207 - 1212
[5] Tetrahedron Asymmetry, 2008, vol. 19, # 17, p. 2072 - 2077

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