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18213-75-7

18213-75-7 Structure

18213-75-7 Structure
IdentificationBack Directory
[Name]

5-Amino-1-methylpyrazole-4-carboxamide
[CAS]

18213-75-7
[Synonyms]

BUTTPARK 94\04-11
5-AMINO-1-METHYLPYRAZOLE-4-CARBOXAMIDE
5-amino-1-methyl-4-pyrazolecarboxamide
5-AMINO-1-METHYL-1H-PYRAZOLE-4-CARBOXAMIDE
5-Amino-1-methylpyrazole-4-carboxamide, tech
1H-Pyrazole-4-carboxaMide, 5-aMino-1-Methyl-
5-Amino-1,3-dimethyl-1H-pyrazole-4-carboxamide
5-Amino-1-methyl-1h-pyrazole-4-carboxamide, tech
1H-Pyrazole-4-carboxamide,5-amino-1-methyl-(9CI)
5-AMINO-1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID AMIDE
3-imino-2-methyl-2,3-dihydro-1H-pyrazole-4-carboxamide
5-amino-1-methyl-1H-pyrazole-4-carboxamide(SALTDATA: FREE)
5-Amino-4-carbamoyl-1-methyl-1H-pyrazole, 5-Amino-4-(aminocarbonyl)-1-methyl-1H-pyrazole
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C5H8N4O
[MDL Number]

MFCD00111808
[MOL File]

18213-75-7.mol
[Molecular Weight]

140.14
Chemical PropertiesBack Directory
[Melting point ]

224-226°C
[Boiling point ]

355.1±22.0 °C(Predicted)
[density ]

1.56±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

15.26±0.50(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS06
[Signal word ]

Danger
[Hazard statements ]

H301
[Precautionary statements ]

P301+P310
[Hazard Codes ]

Xi,T
[Risk Statements ]

36/37/38-25
[Safety Statements ]

26-36/37/39-24/25-22-45
[RIDADR ]

UN 2811 6.1 / PGIII
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2933199090
Spectrum DetailBack Directory
[Spectrum Detail]

5-Amino-1-methylpyrazole-4-carboxamide(18213-75-7)MS
5-Amino-1-methylpyrazole-4-carboxamide(18213-75-7)IR1
5-Amino-1-methylpyrazole-4-carboxamide(18213-75-7)IR2
Hazard InformationBack Directory
[Synthesis]

1-Methyl-4-cyano-5-amino-1,2-pyrazole

5334-41-8

5-Amino-1-methylpyrazole-4-carboxamide

18213-75-7

The general procedure for the synthesis of 5-amino-1-methyl-1H-pyrazole-4-carboxamide from 1-methyl-4-cyano-5-amino-1,2-pyrazole was carried out as follows: a mixture of 1-methyl-4-cyano-5-amino-1,2-pyrazole (0.11 mol) and concentrated sulfuric acid (30 mL, 0.6 mol) was stirred for 1 h at room temperature. Upon completion of the reaction, the mixture was slowly poured into ice water and the pH was adjusted to 8 with 50% aqueous ammonium hydroxide under ice bath conditions.Subsequently, the precipitated solid product was filtered and washed with cold water to give the final 5-amino-1-methyl-1H-pyrazole-4-carboxamide (13.5 g, 91% yield).

[References]

[1] Patent: WO2009/97446, 2009, A1. Location in patent: Page/Page column 64
[2] Patent: WO2009/97446, 2009, A1. Location in patent: Page/Page column 64
[3] Journal of Organic Chemistry, 1956, vol. 21, p. 1240,1242
[4] Patent: EP2025678, 2009, A1. Location in patent: Page/Page column 18-19
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