ChemicalBook--->CAS DataBase List--->25900-61-2

25900-61-2

25900-61-2 Structure

25900-61-2 Structure
IdentificationMore
[Name]

3-AMINOBENZOYLMETHYLAMIDE
[CAS]

25900-61-2
[Synonyms]

3-AMINOBENZOYLMETHYLAMIDE
3-AMINO-N-METHYLBENZAMIDE
BUTTPARK 25\02-27
Benzamide, 3-amino-N-methyl-(9CI)
3-AMINOBENZOYLMETHYLAMIDE 98+%
N-Methyl-3-aminobenzamide
[EINECS(EC#)]

233-675-7
[Molecular Formula]

C8H10N2O
[MDL Number]

MFCD00070630
[Molecular Weight]

150.18
[MOL File]

25900-61-2.mol
Chemical PropertiesBack Directory
[Melting point ]

119°C
[Boiling point ]

346.7±25.0 °C(Predicted)
[density ]

1.137±0.06 g/cm3(Predicted)
[storage temp. ]

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

powder to crystaline
[pka]

15.19±0.46(Predicted)
[color ]

White to Light yellow to Light red
[CAS DataBase Reference]

25900-61-2(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[WGK Germany ]

3
[HS Code ]

2924.29.7790
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

3-AMINOBENZOYLMETHYLAMIDE(25900-61-2)MS
3-AMINOBENZOYLMETHYLAMIDE(25900-61-2)1HNMR
Well-known Reagent Company Product InformationBack Directory
[TCI AMERICA]

3-Amino-N-methylbenzamide,>98.0%(LC)(25900-61-2)
Hazard InformationBack Directory
[Synthesis]

N-methyl-3-nitrobenzamide

3400-26-8

3-AMINOBENZOYLMETHYLAMIDE

25900-61-2

General procedure for the synthesis of 3-amino-N-methylbenzamide from N-methyl-3-nitrobenzamide: A mixture of N-methyl-3-nitrobenzamide (2.47 g, 13.71 mmol) with 10% Pd/C catalyst (0.5 g) in methanol (50 mL) was subjected to hydrogenation at room temperature and atmospheric pressure overnight. Upon completion of the reaction, the mixture was filtered through a diatomaceous earth pad and the filtrate was subsequently concentrated. The resulting crude product was used directly in the subsequent reaction steps without further purification. (Yield: 2.06 g, 100%)

[References]

[1] Patent: US2004/97493, 2004, A1. Location in patent: Page/Page column 24
[2] Patent: US2010/160323, 2010, A1. Location in patent: Page/Page column 54
[3] Journal of Chemical Research, 2006, # 4, p. 223 - 224
[4] Patent: US5589489, 1996, A
[5] Patent: EP2774918, 2014, A1. Location in patent: Paragraph 0126; 0133
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