Basic information Safety Supplier Related

5-AMINO-3-ETHYL-1H-PYRAZOLE

Basic information Safety Supplier Related

5-AMINO-3-ETHYL-1H-PYRAZOLE Basic information

Product Name:
5-AMINO-3-ETHYL-1H-PYRAZOLE
Synonyms:
  • 5-AMINO-3-ETHYL-1H-PYRAZOLE
  • 5-ETHYL-2H-PYRAZOL-3-YLAMINE
  • 5-ethyl-3-aMino-1H-pyrazole
  • 3-Amino-5-ethyl-2H-pyrazole
  • 3-Ethyl-1H-pyrazol-5-amine hydrochloride
  • H50782
  • 1H-Pyrazol-3-amine, 5-ethyl-
  • 3-AMino-5-ethylpyrazole
CAS:
1904-24-1
MF:
C5H9N3
MW:
111.15
Mol File:
1904-24-1.mol
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5-AMINO-3-ETHYL-1H-PYRAZOLE Chemical Properties

Boiling point:
313.8±22.0 °C(Predicted)
Density 
1.126 g/mL at 25 °C
refractive index 
1.5420
Flash point:
>110℃
storage temp. 
Keep in dark place,Sealed in dry,Store in freezer, under -20°C
form 
solid
pka
15.84±0.10(Predicted)
Appearance
Light yellow to yellow Liquid
InChI
InChI=1S/C5H9N3/c1-2-4-3-5(6)8-7-4/h3H,2H2,1H3,(H3,6,7,8)
InChIKey
AXDGPQLEVYSXNL-UHFFFAOYSA-N
SMILES
N1C(CC)=CC(N)=N1
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36/37/38
Safety Statements 
23-26-36/37/39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933199090
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5-AMINO-3-ETHYL-1H-PYRAZOLE Usage And Synthesis

Uses

3-Amino-5-ethyl-1H-pyrazole is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

Definition

ChEBI: 3-Amino-5-ethyl-1H-pyrazole is a dicarboximide and a heterocyclic compound.

Synthesis

33279-01-5

1904-24-1

GENERAL STEPS: 3-Oxopentanenitrile (XXXV; 2 g; 21 mmol) was dissolved in ethanol (60 mL) under stirring conditions, followed by the addition of hydrazine hydrate (1.3 mL; 41 mmol). The reaction mixture was heated to reflux for 12 hours. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated under reduced pressure. The crude product was purified by column chromatography (eluent: 8% methanol-dichloromethane) to afford 5-ethyl-1H-pyrazol-3-amine (XXXVI; 1.8 g; 78% yield) as a brown viscous solid. The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6): δ 11.0 (broad single peak, 1H), 5.17 (single peak, 1H), 4.5 (broad single peak, 2H), 2.4 (multiple peaks, 2H), and 1.1 (triple peak, 3H). Mass spectrometry analysis showed a molecular ion peak (M+1) of 111.93.

References

[1] Patent: WO2015/97122, 2015, A1. Location in patent: Page/Page column 92
[2] Patent: WO2007/99326, 2007, A1. Location in patent: Page/Page column 114

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