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N-Methoxy-N,2,2-trimethylpropanamide

CAS No.
64214-60-4
Chemical Name:
N-Methoxy-N,2,2-trimethylpropanamide
Synonyms
N-Methoxy-N,2,2-trimethylpropanamide;Propanamide, N-methoxy-N,2,2-trimethyl-
CBNumber:
CB42565293
Molecular Formula:
C7H15NO2
Molecular Weight:
145.2
MDL Number:
MFCD11847426
MOL File:
64214-60-4.mol
Last updated:2025-07-24 18:13:52
Product description Number Pack Size Price
N-Methoxy-N,2,2-trimethylpropanamide M268780 1g $175
N-Methoxy-N-methylpivalamide 9831AB 5g $411
N-Methoxy-N-methylpivalamide 188534 5g $478
N-Methoxy-N-methylpivalamide 188534 10g $833
N-Methoxy-N-methylpivalamide 188534 25g $1666

N-Methoxy-N,2,2-trimethylpropanamide Properties

Boiling point 62-64 °C(Press: 10 Torr)
Density 0.937±0.06 g/cm3(Predicted)
storage temp. 2-8°C
Appearance Colorless to light yellow Liquid

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302+H312+H332
Precautionary statements  P501-P261-P270-P271-P264-P280-P362+P364-P301+P312+P330-P302+P352+P312-P304+P340+P312
HS Code  2928009090

N-Methoxy-N,2,2-trimethylpropanamide price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC M268780 N-Methoxy-N,2,2-trimethylpropanamide 64214-60-4 1g $175 2021-12-16 Buy
AK Scientific 9831AB N-Methoxy-N-methylpivalamide 64214-60-4 5g $411 2021-12-16 Buy
Matrix Scientific 188534 N-Methoxy-N-methylpivalamide 64214-60-4 5g $478 2021-12-16 Buy
Matrix Scientific 188534 N-Methoxy-N-methylpivalamide 64214-60-4 10g $833 2021-12-16 Buy
Matrix Scientific 188534 N-Methoxy-N-methylpivalamide 64214-60-4 25g $1666 2021-12-16 Buy
Product number Packaging Price Buy
M268780 1g $175 Buy
9831AB 5g $411 Buy
188534 5g $478 Buy
188534 10g $833 Buy
188534 25g $1666 Buy

N-Methoxy-N,2,2-trimethylpropanamide Chemical Properties,Uses,Production

Synthesis

N-methoxymethylamine

1117-97-1

Pivalic acid

75-98-9

N-Methoxy-N,2,2-trimethylpropanamide

64214-60-4

GENERAL PROCEDURE: Methoxymethylamine (0.360 g, 6.0 mmol) and valproic acid (0.244 g, 2.0 mmol) were dissolved in anhydrous toluene (10 mL) and stirred for 10 min at 0 °C. Subsequently, a solution of phosphorus trichloride (0.137 g, 1.0 mmol) in anhydrous toluene (2 mL) was slowly added dropwise to the reaction mixture. After the dropwise addition, the reaction mixture was gradually warmed up to room temperature and stirring was continued for 0.5 h at 60 °C. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the completion of the reaction, the mixture was cooled to room temperature. The reaction was quenched with saturated sodium bicarbonate solution (20 mL) and subsequently extracted with ethyl acetate (3 x 10 mL). The organic phases were combined and dried over anhydrous magnesium sulfate. The solvent was removed by concentration under reduced pressure to give the crude product. The crude product was purified by column chromatography (silica gel, petroleum ether-ethyl acetate, 3:2) to afford N-methoxy-N,2,2-trimethylpropionamide (3a) as a colorless oil. Yield: 320 mg (97%).

References

[1] Synthesis (Germany), 2014, vol. 46, # 3, p. 320 - 330
[2] Journal of Organic Chemistry, 2004, vol. 69, # 25, p. 8984 - 8986

N-Methoxy-N,2,2-trimethylpropanamide Preparation Products And Raw materials

N-Methoxy-N,2,2-trimethylpropanamide Suppliers

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N-Methoxy-N,2,2-trimethylpropanamide Spectrum

N-Methoxy-N,2,2-trimethylpropanamide Propanamide, N-methoxy-N,2,2-trimethyl- 64214-60-4