ChemicalBook--->CAS DataBase List--->22356-89-4

22356-89-4

22356-89-4 Structure

22356-89-4 Structure
IdentificationBack Directory
[Name]

2-Amino-N-methyl-acetamide
[CAS]

22356-89-4
[Synonyms]

Einecs 244-934-9
Glycine MethylaMide
Acetamide, 2-amino-N-methyl-
Aminoacetic acid methyl amide
N~1~-methylglycinamide hydrochloride
N~1~-methylglycinamide(SALTDATA: HCl)
[EINECS(EC#)]

244-934-9
[Molecular Formula]

C3H8N2O
[MDL Number]

MFCD06375945
[MOL File]

22356-89-4.mol
[Molecular Weight]

88.11
Chemical PropertiesBack Directory
[Boiling point ]

275.6±23.0 °C(Predicted)
[density ]

1.005±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[pka]

15.37±0.46(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302+H312+H332-H315
[Precautionary statements ]

P280-P301+P312-P362+P364
[HS Code ]

2924190090
Spectrum DetailBack Directory
[Spectrum Detail]

2-Amino-N-methyl-acetamide(22356-89-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

N-Methyl Cbz-GlycinaMide

21855-72-1

2-Amino-N-methyl-acetamide

22356-89-4

The general procedure for the synthesis of 2-amino-N-methylacetamide from compound 12a (CAS:21855-72-1) was as follows: 10% Pd/C catalyst was added to a methanol (10 mL) solution of compound 12a (170 mg, 0.77 mmol). The hydrogenation reaction was carried out at room temperature and atmospheric pressure for 3 hours. Upon completion of the reaction, the catalyst was removed by diatomaceous earth filtration and the resulting clarified solution was dried to give 2-amino-N-methylacetamide as an oily product. The yield was 97%. The molecular formula is C3H9N2O.

[References]

[1] Patent: WO2006/103463, 2006, A1. Location in patent: Page/Page column 15; Figure 3
[2] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 3, p. 1285 - 1297
[3] Journal of Organic Chemistry, 1977, vol. 42, # 12, p. 2105 - 2108
[4] Synthesis, 1977, p. 478 - 480
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