ChemicalBook--->CAS DataBase List--->1187-59-3

1187-59-3

1187-59-3 Structure

1187-59-3 Structure
IdentificationBack Directory
[Name]

N-METHYLACRYLAMIDE
[CAS]

1187-59-3
[Synonyms]

n-methyl-acrylamid
N-METHYLACRYLAMIDE
n-methyl-2-propenamid
N-methyl-2-Propenamide
N-methylprop-2-enamide
2-Propenamide,N-methyl-
[EINECS(EC#)]

214-700-0
[Molecular Formula]

C4H7NO
[MDL Number]

MFCD00053693
[MOL File]

1187-59-3.mol
[Molecular Weight]

85.1
Chemical PropertiesBack Directory
[Melting point ]

102-106 °C
[Boiling point ]

156.6°C (rough estimate)
[density ]

1.0408 (rough estimate)
[refractive index ]

1.4340 (estimate)
[storage temp. ]

Sealed in dry,2-8°C
[pka]

15.12±0.46(Predicted)
[Appearance]

Colorless to light yellow Liquid
[CAS DataBase Reference]

1187-59-3
[EPA Substance Registry System]

2-Propenamide, N-methyl- (1187-59-3)
Safety DataBack Directory
[Risk Statements ]

20/21/22-36/37/38
[Safety Statements ]

23-26-36/37/39
[RIDADR ]

2810
[TSCA ]

TSCA listed
[HazardClass ]

6.1(b)
[PackingGroup ]

III
[Safety Profile]

Moderately toxic by ingestion. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.
Spectrum DetailBack Directory
[Spectrum Detail]

N-METHYLACRYLAMIDE(1187-59-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-methoxy-N-methylpropanamide

38188-92-0

N-METHYLACRYLAMIDE

1187-59-3

(C) To a 1000 mL four-necked flask equipped with a stirrer, thermometer, and gas introduction tube was added 400 g of MeO-DEAA obtained in step (b), followed by 6.8 g of potassium hydroxide and 0.4 g of TDA.A distillation column equipped with a packer, condenser, and distillation receiver was mounted on the flask, and a trace amount of nitrogen was passed through to act as a carrier gas. The reaction temperature was adjusted to 180 °C while stirring the reaction mixture. The system vacuum was adjusted to 60 kPa and the pyrolysis reaction was carried out for 12 hours. 307 g of crude N,N-diethylacrylamide (DEAA) (purity = 93%, yield = 92%) was obtained by collection through a water condenser. The crude DEAA was transferred to a distillation purification unit equipped with a 20 cm McMahon packing (6 mm particle size) filled column and purified by reduced pressure distillation (60 °C/0.13 kPa). The final 258 g of high purity DEAA (99.8% purity) was obtained as a colorless liquid. Examples 2-18: On the basis of Example 1, the raw materials, catalysts, solvents, polymerization blockers and reaction conditions were varied as shown in Table 1 and synthesized according to the same steps as in Example 1 to obtain the corresponding N-methyl-2-acrylamide. The results are summarized in Table 2.

[References]

[1] Patent: JP2015/101554, 2015, A. Location in patent: Paragraph 0057; 0060
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