ChemicalBook--->CAS DataBase List--->28466-26-4

28466-26-4

28466-26-4 Structure

28466-26-4 Structure
IdentificationBack Directory
[Name]

1H-PYRAZOL-4-YLAMINE
[CAS]

28466-26-4
[Synonyms]

AKOS PAO-0001
4-AMINOPYRAZOLE
1H-Pyrazol-4-amine
4-Aminopyrazole 95%
4-AMINO-1H-PYRAZOLE
1H-Pyrazole-4-amine
H-PYRAZOL-4-YLAMINE
1H-PYRAZOL-4-YLAMINE
[EINECS(EC#)]

625-292-2
[Molecular Formula]

C3H5N3
[MDL Number]

MFCD01693729
[MOL File]

28466-26-4.mol
[Molecular Weight]

83.0919
Questions And AnswerBack Directory
[Form]

powder
Chemical PropertiesBack Directory
[Melting point ]

75-77°C
[Boiling point ]

142.17°C (rough estimate)
[density ]

1.0248 (rough estimate)
[refractive index ]

1.5060 (estimate)
[storage temp. ]

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
[form ]

powder to crystal
[pka]

17.70±0.50(Predicted)
[color ]

White to Brown to Dark purple
[Sensitive ]

Hygroscopic
[InChI]

InChI=1S/C3H5N3/c4-3-1-5-6-2-3/h1-2H,4H2,(H,5,6)
[InChIKey]

AXINVSXSGNSVLV-UHFFFAOYSA-N
[SMILES]

N1C=C(N)C=N1
[CAS DataBase Reference]

28466-26-4
[NIST Chemistry Reference]

4-NH2-pyrazole(28466-26-4)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P301+P312-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

22-36/37/38
[Safety Statements ]

26-36/37
[WGK Germany ]

3
[RTECS ]

UQ4993000
[HazardClass ]

IRRITANT
[HS Code ]

2933199090
Hazard InformationBack Directory
[Uses]

4-Aminopyrazole, is a versatile building block for the preparation of pharmaceutical and biologically active compounds. 4-Amino-1H-pyrazole, has also shown to have anticonvulsant activity, and thus can be used in the treatment of epileptic seizures.
[Synthesis]

4-Nitropyrazole

2075-46-9

1H-PYRAZOL-4-YLAMINE

28466-26-4

4-Nitropyrazole (1.13 g, 10 mmol) was dissolved in methanol (10 mL) under hydrogen (1 atm) atmosphere and 10% Pd-C catalyst (0.1 g) was added. The reaction mixture was stirred at 25 °C for 12 hours. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to afford the target product 4-aminopyrazole (860 mg, yield: 100%), which could be used in subsequent reactions without further purification.

[References]

[1] Patent: US2015/336982, 2015, A1. Location in patent: Paragraph 0252; 0253
[2] ChemMedChem, 2016, p. 1695 - 1699
[3] Patent: CN105418616, 2016, A. Location in patent: Paragraph 0118; 0119
[4] Organic and Biomolecular Chemistry, 2013, vol. 11, # 3, p. 395 - 399
[5] Patent: WO2017/178510, 2017, A1. Location in patent: Page/Page column 297
Spectrum DetailBack Directory
[Spectrum Detail]

1H-PYRAZOL-4-YLAMINE(28466-26-4)1HNMR
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