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3-Amino-5-phenylpyrazole

Basic information Safety Supplier Related

3-Amino-5-phenylpyrazole Basic information

Product Name:
3-Amino-5-phenylpyrazole
Synonyms:
  • SALOR-INT L317837-1EA
  • 5-amino-3-phenyl-pyrazol
  • JR-8809, 5-Phenyl-1H-pyrazole-3-ylamine, 97%
  • 5-PHENYL-2H-PYRAZOL-3-YLAMINE
  • 5-PHENYL-1H-PYRAZOL-3-AMINE
  • 5-PHENYL-1H-PYRAZOL-3-YLAMINE
  • AKOS B003768
  • AKOS 92617
CAS:
1572-10-7
MF:
C9H9N3
MW:
159.19
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Imidazoles, Pyrroles, Pyrazoles, Pyrrolidines
  • Heterocyclic Compounds
  • Pyrazoles
  • pyrazole series
Mol File:
1572-10-7.mol
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3-Amino-5-phenylpyrazole Chemical Properties

Melting point:
124-127 °C (lit.)
Boiling point:
442.3±33.0 °C(Predicted)
Density 
1.238±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
DMSO, Methanol
pka
14.80±0.10(Predicted)
form 
Powder or Crystals
color 
Red to brown
BRN 
4947
InChIKey
PWSZRRFDVPMZGM-UHFFFAOYSA-N
CAS DataBase Reference
1572-10-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
RTECS 
UQ6109000
Hazard Note 
Irritant
HS Code 
29331990
Toxicity
mouse,LDLo,intraperitoneal,630mg/kg (630mg/kg),Farmakologiya i Toksikologiya Vol. 27, Pg. 295, 1964.

MSDS

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3-Amino-5-phenylpyrazole Usage And Synthesis

Chemical Properties

Off-white to cream colored crystalline powder

Uses

3-Amino-5-phenylpyrazole ((3-phenyl-1H-pyrazol-5-amine) may be used in the synthesis of the following:

  • Urea derivatives by reaction with azido(6-(benzofuran-2-yl)-2-methylpyridin-3-yl) methanone.
  • 2-Mercaptoacetamide analogs by treating with thioglycolic acid.
  • 3-(Substituentpyrimidayl)-5,6-benzocoumarins by treating with 3-(2′-formyl-1′-chlorovinyl)-5,6-benzocoumarin.
  • Substituted 2,7-diphenylpyrazolo[1,5-a]pyrimidine-5-carboxylic esters by reacting with substituted β-diketo esters.
  • N-ethoxycarbonylthiourea derivative by reacting with ethoxycarbonyl isothiocyanate.
  • Heterobiaryl pyrazolo[3,4-b]pyridines by reacting with indole-3-carboxaldehyde.

General Description

3-Amino-5-phenylpyrazole (3-phenyl-1H-pyrazol-5-amine), an amino pyrazole derivative, is an aza-heterocyclic amine. It has been reported to be synthesized by heating either 3-amino-4-bromo- or 3-amino-5-phenylisothiazole in the presence of anhydrous hydrazine. On reaction with ZnCl2 it affords chlorido-tris(3-amino-5-phenyl-1Hpyrazole-N2)zinc (II) chloride.

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