Basic information Safety Supplier Related

5-(4-NITRO-PHENYL)-2H-TETRAZOLE

Basic information Safety Supplier Related

5-(4-NITRO-PHENYL)-2H-TETRAZOLE Basic information

Product Name:
5-(4-NITRO-PHENYL)-2H-TETRAZOLE
Synonyms:
  • BUTTPARK 2\01-81
  • 5-(4-NITROPHENYL)TETRAZOLE
  • 5-(4-NITRO-PHENYL)-2H-TETRAZOLE
  • 5-(4-NITROPHENYL)-1H-TETRAZOLE
  • 5-(4-nitrophenyl)-2H-1,2,3,4-tetrazole
  • 4-(1H-Tetrazol-5-yl)nitrobenzene
  • 2H-Tetrazole, 5-(4-nitrophenyl)-
CAS:
16687-60-8
MF:
C7H5N5O2
MW:
191.15
Mol File:
16687-60-8.mol
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5-(4-NITRO-PHENYL)-2H-TETRAZOLE Chemical Properties

Melting point:
223°C (dec.)
Boiling point:
435.3±47.0 °C(Predicted)
Density 
1.534±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
3.38±0.10(Predicted)
Appearance
Yellow to brown Solid
Water Solubility 
Insoluble in water. Soluble in DMSO.
BRN 
192840
CAS DataBase Reference
16687-60-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
Hazard Note 
Irritant
HS Code 
2933998090

MSDS

  • Language:English Provider:ALFA
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5-(4-NITRO-PHENYL)-2H-TETRAZOLE Usage And Synthesis

Uses

It is used as a reagent used as activator for both solution- and solid-phase synthesis of oligonucleotides using the phosphoramidite method.

Synthesis

1129-37-9

16687-60-8

The general procedure for the synthesis of 5-(4-nitrophenyl)-1H-tetrazole from 4-nitrophenyl aldoxime was as follows: InCl3 (3 mol%) was added to a stirred solution of DMF (5 mL) containing appropriate amounts of aldoxime (1 mmol) and NaN3 (1.5 mmol). The reaction mixture was heated to 120 °C. After completion of the reaction (monitored by TLC), the mixture was cooled to room temperature. H2O (5 mL), 2M HCl aqueous solution (10 mL) and EtOAc (10 mL) were added sequentially with vigorous stirring for 15 minutes. The organic layer was separated and the aqueous layer was extracted with EtOAc (3 x 15 mL). The organic extracts were combined, washed with H2O, dried over anhydrous Na2SO4 and filtered. The solvent was evaporated under reduced pressure and the crude product was purified by silica gel column chromatography [eluent: EtOAc-hexane (9:1)].

References

[1] Synlett, 2016, vol. 27, # 8, p. 1241 - 1244
[2] Tetrahedron Letters, 2012, vol. 53, # 29, p. 3706 - 3709
[3] Synthesis (Germany), 2018, vol. 50, # 6, p. 1293 - 1300
[4] Synlett, 2016, vol. 27, # 15, p. 2225 - 2228
[5] Tetrahedron Letters, 2016, vol. 57, # 5, p. 523 - 524

5-(4-NITRO-PHENYL)-2H-TETRAZOLESupplier

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