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4-(1H-Pyrazol-1-yl)aniline

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Products Intro: Product Name:4-1H-Pyrazol-1-yl-phenylamine
CAS:17635-45-9
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:17635-45-9
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CAS:17635-45-9
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CAS:17635-45-9
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-69841
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Products Intro: Product Name:4-(1h-pyrazol-1-yl)aniline
CAS:17635-45-9
Purity:0.99 Package:1kg

4-(1H-Pyrazol-1-yl)aniline manufacturers

  • 4-Pyrazol-1-yl-phenylamine
  • 4-Pyrazol-1-yl-phenylamine pictures
  • $0.00 / 1KG
  • 2022-01-04
  • CAS:17635-45-9
  • Min. Order: 1g
  • Purity: 98%min
  • Supply Ability: 4-Pyrazol-1-yl-phenylamine
4-(1H-Pyrazol-1-yl)aniline Basic information
Product Name:4-(1H-Pyrazol-1-yl)aniline
Synonyms:CHEMBRDG-BB 4102901;BUTTPARK 98\50-47;1-(4-AMINOPHENYL)PYRAZOLE;4-PYRAZOL-1-YL-PHENYLAMINE;4-PYRAZOL-1-YL-PHENYLAMINE HCL;4-PYRAZOL-1-YL-PHENYLAMINE HYDROCHLORIDE;4-(1H-PYRAZOL-1-YL)ANILINE;AKOS B029459
CAS:17635-45-9
MF:C9H9N3
MW:159.19
EINECS:
Product Categories:Amines and Anilines;Heterocycles
Mol File:17635-45-9.mol
4-(1H-Pyrazol-1-yl)aniline Structure
4-(1H-Pyrazol-1-yl)aniline Chemical Properties
Melting point 54 °C
Boiling point 312.0±25.0 °C(Predicted)
density 1.20±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
form solid
pka4.03±0.10(Predicted)
AppearanceGray to brown Solid
InChIInChI=1S/C9H9N3/c10-8-2-4-9(5-3-8)12-7-1-6-11-12/h1-7H,10H2
InChIKeyCSFIQHZIFKIQNO-UHFFFAOYSA-N
SMILESC1(N)=CC=C(N2C=CC=N2)C=C1
CAS DataBase Reference17635-45-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39-37/39
WGK Germany WGK 3
HazardClass IRRITANT
HS Code 2921420090
Storage Class11 - Combustible Solids
MSDS Information
4-(1H-Pyrazol-1-yl)aniline Usage And Synthesis
Synthesis
1-(4-Nitrophenyl)-1H-pyrazole

3463-30-7

4-(1H-Pyrazol-1-yl)aniline

17635-45-9

GENERAL STEPS: In a typical reaction, 5.0 mg of Pd-gCN catalyst (containing 5.0 wt% Pd) was mixed with 1.0 mM 1-(4-nitrophenyl)-1H-pyrazole in ethanol (2 mL) and 60% hydrazine hydrate solution (2 mM, 1.2 equiv, 0.07 mL). The mixture was placed in a 10 mL round-bottomed flask and reacted at reflux temperature (70°C) for 4 hours, followed by cooling to room temperature. After completion of the reaction, the reaction mixture was filtered and the filtrate was purified by silica gel column chromatography to afford 4-(1H-pyrazol-1-yl)aniline (1-(4-aminophenyl)pyrazole). For dinitroaromatic substrates, 4.0 mM (2.4 eq., 0.14 mL) of 60% hydrazine hydrate solution is required.

References[1] Chemical and Pharmaceutical Bulletin, 2000, vol. 48, # 12, p. 1935 - 1946
[2] Applied Catalysis A: General, 2016, vol. 523, p. 31 - 38
[3] Patent: EP3159340, 2017, A1. Location in patent: Paragraph 0086; 0091
[4] Patent: US2015/336982, 2015, A1. Location in patent: Paragraph 0165; 0167
[5] Patent: CN105418590, 2016, A. Location in patent: Paragraph 0152; 0153; 0154
4-(1H-Pyrazol-1-yl)aniline Preparation Products And Raw materials
Raw materials1-(4-Nitrophenyl)-1H-pyrazole-->Pyrazole-->4-Bromoaniline-->4-Iodoaniline-->Hydrazine hydrate-->Ethanol
Tag:4-(1H-Pyrazol-1-yl)aniline(17635-45-9) Related Product Information
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