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Chemical Structure| 3179-31-5 Chemical Structure| 3179-31-5
Chemical Structure| 3179-31-5

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Product Details of 3-Mercapto-1,2,4-triazole

CAS No. :3179-31-5
Formula : C2H3N3S
M.W : 101.13
SMILES Code : SC1=NNC=N1
MDL No. :MFCD00005229
InChI Key :AFBBKYQYNPNMAT-UHFFFAOYSA-N
Pubchem ID :2723802

Safety of 3-Mercapto-1,2,4-triazole

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H319
Precautionary Statements:P305+P351+P338

Application In Synthesis of 3-Mercapto-1,2,4-triazole

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 3179-31-5 ]

[ 3179-31-5 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 3034-48-8 ]
  • [ 3179-31-5 ]
  • [ 79134-06-8 ]
  • 2
  • [ 13421-00-6 ]
  • [ 3179-31-5 ]
  • 7-chloro-9H-[1,2,4]triazolo[5,1-b][1,3]benzothiazin-9-one [ No CAS ]
  • 3
  • [ 19230-50-3 ]
  • [ 3179-31-5 ]
  • 7-nitro-9H-[1,2,4]triazolo[5,1-b][1,3]benzothiazin-9-one [ No CAS ]
  • 4
  • [ 13421-00-6 ]
  • [ 3179-31-5 ]
  • 7-chloro-9H-[1,2,4]triazolo[5,1-b][1,3]benzothiazin-9-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
80% With potassium carbonate; In N,N,N,N,N,N-hexamethylphosphoric triamide; at 80℃; for 24h;Sealed tube; Schlenk technique; Schlenk reaction tube, <strong>[13421-00-6]5-chloro-2-iodo<strong>[13421-00-6]benzoic acid</strong></strong> (0.5 mmol), 3-mercapto 1,2,4-triazole (0.5 mmol), potassium carbonate (0.1 mmol) and HMPA 2 mL). The reaction tube was sealed and reacted at 80 C for 24 hours under an air atmosphere. After completion of the reaction, acetic acid (1 ml) was added, stirred at room temperature for 1 hour, then extracted twice with methylene chloride. The organic layer was washed three times with saturated brine. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. And purified by column chromatography to obtain product 3. The structure and characterization data are as follows
  • 5
  • [ 19230-50-3 ]
  • [ 3179-31-5 ]
  • 7-nitro-9H-[1,2,4]triazolo[5,1-b][1,3]benzothiazin-9-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
71% With potassium carbonate; In N,N,N,N,N,N-hexamethylphosphoric triamide; at 80℃; for 24h;Sealed tube; Schlenk technique; Schlenk reaction tube A solution of <strong>[19230-50-3]5-nitro-2-iodobenzoic acid</strong> (0.5 mmol), 3-mercapto 1,2,4-triazole (0.5 mmol), potassium carbonate (0.1 mmol) and HMPA (2 mL). The reaction tube was sealed and reacted at 80 C for 24 hours under an air atmosphere. After completion of the reaction, acetic acid (1 ml) was added, stirred at room temperature for 1 hour, then extracted twice with methylene chloride. The organic layer was washed three times with saturated brine. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. And purified by column chromatography to obtain the product 5, and its structure and characterization data are as follows
 

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