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1-Methyl-1,2,3-triazole

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1-Methyl-1,2,3-triazole Basic information

Product Name:
1-Methyl-1,2,3-triazole
Synonyms:
  • 1-Methyl-1,2,3-triazole
  • NISTC16681655
  • 1H-1,2,3-Triazole, 1-methyl-
  • 1-Methyl-1
  • 1-Methyl-1,2,3-triazole CAS:16681-65-5
  • methyltriazole
CAS:
16681-65-5
MF:
C3H5N3
MW:
83.09
Mol File:
16681-65-5.mol
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1-Methyl-1,2,3-triazole Chemical Properties

Boiling point:
223-225 °C
Density 
1.17±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
1.40±0.10(Predicted)
Appearance
Colorless to light yellow Liquid
InChI
InChI=1S/C3H5N3/c1-6-3-2-4-5-6/h2-3H,1H3
InChIKey
JWAWEQBUZOGIBZ-UHFFFAOYSA-N
SMILES
N1(C)C=CN=N1
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Safety Information

HazardClass 
IRRITANT
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1-Methyl-1,2,3-triazole Usage And Synthesis

Uses

An azole compound used for binding affinity with various cytochrome P 450 (CYP) proteins.

Synthesis

288-36-8

74-88-4

16681-65-5

Step A: 1H-1,2,3-triazole (1.0 g, 14.5 mmol), iodomethane (3.1 g, 21.7 mmol), and potassium carbonate (4.0 g, 28.9 mmol) were dissolved in tetrahydrofuran (15 mL), and the reaction was stirred for 3 hours at room temperature. After the reaction was completed, ethyl acetate (20 mL) and water (10 mL) were added for extraction and the organic phase was separated. The organic phase was concentrated under reduced pressure to remove the solvent to obtain the crude product. The crude product was purified by silica gel column chromatography with 10% methanol/dichloromethane as eluent to afford 1-methyl-1H-1,2,3-triazole (860 mg, 10.4 mmol, 71% yield) as a yellow oil.

References

[1] Crystal Growth and Design, 2015, vol. 15, # 2, p. 752 - 758
[2] Chemistry - A European Journal, 2017, vol. 23, # 71, p. 17870 - 17873
[3] Patent: WO2015/142903, 2015, A2. Location in patent: Page/Page column 102
[4] Patent: WO2015/140133, 2015, A1. Location in patent: Page/Page column 115
[5] ACS Medicinal Chemistry Letters, 2015, vol. 6, # 6, p. 650 - 654

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