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24549-12-0

24549-12-0 Structure

24549-12-0 Structure
IdentificationBack Directory
[Name]

methyl 3-(methylamino)propanoate
[CAS]

24549-12-0
[Synonyms]

methyl 3-(methylamino)propanoate
β-Alanine, N-methyl-, methyl ester
[Molecular Formula]

C5H11NO2
[MDL Number]

MFCD11505527
[MOL File]

24549-12-0.mol
[Molecular Weight]

117.15
Chemical PropertiesBack Directory
[Boiling point ]

50 °C(Press: 11 Torr)
[density ]

0.949±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Store in freezer, under -20°C
[pka]

9.39±0.10(Predicted)
[Appearance]

Colorless to light yellow Liquid
[InChI]

InChI=1S/C5H11NO2/c1-6-4-3-5(7)8-2/h6H,3-4H2,1-2H3
[InChIKey]

NGNUXOCKVMKGQL-UHFFFAOYSA-N
[SMILES]

C(OC)(=O)CCNC
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)Exclamation Mark (GHS07)Corrosion (GHS05)
GHS02,GHS07,GHS05
[Signal word ]

Danger
[Hazard statements ]

H318-H315-H226-H335-H302
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P280-P305+P351+P338-P310-P264-P270-P301+P312-P330-P501
[HS Code ]

2922498590
Spectrum DetailBack Directory
[Spectrum Detail]

methyl 3-(methylamino)propanoate(24549-12-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

acrylic acid methyl ester

292638-85-8

Methylamine

74-89-5

methyl 3-(methylamino)propanoate

24549-12-0

Example 38: General procedure for the synthesis of methyl 3-(methylamino)propionate: methyl acrylate (10 g, 116 mmol) was dissolved in methanol (20 mL) and the solution was cooled to -20 °C. Methylamine solution (2M, dissolved in tetrahydrofuran, 90mL, 180mmol) was added slowly through the addition funnel, keeping the reaction mixture stirred at -20°C for 2 hours. After completion of the reaction, the solvent was removed under vacuum. The residue was distilled under reduced pressure (45 °C, 5 Torr) to give methyl 3-(methylamino)propionate as a colorless liquid (3.5 g, 28% yield). The product was characterized by 1H NMR (CDCl3): δ 2.44 (s, 3H), 2.52 (t, 2H, J=6.31Hz), 2.86 (t, 2H, J=6.31Hz), 3.69 (s, 3H).

[References]

[1] Phosphorus, Sulfur and Silicon and Related Elements, 1998, vol. 134-135, p. 231 - 254
[2] Kinetics and Catalysis, 2010, vol. 51, # 5, p. 653 - 656
[3] Organic and Biomolecular Chemistry, 2013, vol. 11, # 12, p. 1929 - 1932
[4] Patent: WO2009/118292, 2009, A1. Location in patent: Page/Page column 74-75
[5] Monatshefte fuer Chemie, 1933, vol. 63, p. 224,230,234
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