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1H-1,2,4-Triazole,1-phenyl-(6CI,7CI,8CI,9CI)

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1H-1,2,4-Triazole,1-phenyl-(6CI,7CI,8CI,9CI) Basic information

Product Name:
1H-1,2,4-Triazole,1-phenyl-(6CI,7CI,8CI,9CI)
Synonyms:
  • 1H-1,2,4-Triazole,1-phenyl-(6CI,7CI,8CI,9CI)
  • 1-Phenyl-1H-1,2,4-triazole
  • 1H-1,2,4-Triazole, 1-phenyl-
  • 1-phenyl-1,2,4-triazole
CAS:
13423-60-4
MF:
C8H7N3
MW:
145.16
Product Categories:
  • TRIAZOLE
Mol File:
13423-60-4.mol
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1H-1,2,4-Triazole,1-phenyl-(6CI,7CI,8CI,9CI) Chemical Properties

Melting point:
47 °C
Boiling point:
268-270 °C
Density 
1.16±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
2.32±0.10(Predicted)
Appearance
Colorless to off-white Solid
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Safety Information

HS Code 
2933998090
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1H-1,2,4-Triazole,1-phenyl-(6CI,7CI,8CI,9CI) Usage And Synthesis

Definition

ChEBI: 1-phenyl-1H-1,2,4-triazole is a member of triazoles.

Synthesis Reference(s)

The Journal of Organic Chemistry, 21, p. 1037, 1956 DOI: 10.1021/jo01115a610

Synthesis

288-88-0

591-50-4

13423-60-4

1. CuI (0.10 g, 0.50 mmol), 1,2,4-triazole (0.69 g, 10 mmol), K3PO4 (4.4 g, 20 mmol), iodobenzene (1.4 mL, 12 mmol), and N,N'-dimethylethylenediamine (0.11 mL, 1.0 mmol) were dissolved in DMF (5 mL) under argon protection. Mixed well and degassed. 2. The reaction mixture was heated and stirred at 110°C for 72 hours. 3. 3. After completion of the reaction, the reaction mixture was filtered through diatomaceous earth and the filter cake was washed with ethyl acetate (AcOEt). 4. The solvent was removed by pressurized distillation to give the crude product. 5. The crude product was purified using silica gel column chromatography with heptane/ethyl acetate (7:3, v/v) as eluent. 6. 1-Phenyl-1H-1,2,4-triazole (2a) was isolated in 96% yield as a yellow powder with a melting point of 48 °C (literature value 28-46 °C). 7. The structure of the product was confirmed by 1H NMR and 13C NMR: 1H NMR (CDCl3, 300 MHz) δ 7.42 (m, 1H), 7.53 (m, 2H), 7.71 (m, 2H), 8.15 (s, 1H), 8.74 (s, 1H); 13C NMR (CDCl3, 75 MHz) δ 120.1 (2CH) , 128.3 (CH), 129.9 (2CH), 137.1 (C), 140.9 (CH), 152.7 (CH).

References

[1] Journal of the American Chemical Society, 2007, vol. 129, # 45, p. 13879 - 13886
[2] Journal of Organic Chemistry, 2007, vol. 72, # 8, p. 2737 - 2743
[3] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 19, p. 6355 - 6363
[4] RSC Advances, 2014, vol. 4, # 83, p. 44105 - 44116
[5] Journal of Organic Chemistry, 2004, vol. 69, # 17, p. 5578 - 5587

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