Basic information Safety Supplier Related

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

Basic information Safety Supplier Related

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

Product Name:
5-(4-BROMO-PHENYL)-2H-TETRAZOLE
Synonyms:
  • JR-6748, 5-(4-Bromophenyl)-1H-tetrazole, 97%
  • BUTTPARK 49\01-68
  • 5-(4-BROMO-PHENYL)-2H-TETRAZOLE
  • 5-(4-BROMOPHENYL)-1H-TETRAZOLE
  • 5-(4-BROMOPHENYL) TETRAZOLE
  • 5-(p-Bromophenyl)-1H-tetrazole
  • 5-(p-Bromophenyl)tetrazole
  • 5-Bromo-2-(tetrazol-5-yl)benzene
CAS:
50907-23-8
MF:
C7H5BrN4
MW:
225.05
EINECS:
622-704-2
Product Categories:
  • Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Tetrazoles
  • TetrazolesHeterocyclic Building Blocks
Mol File:
50907-23-8.mol
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5-(4-BROMO-PHENYL)-2H-TETRAZOLE Chemical Properties

Melting point:
260 °C (dec.)(lit.)
Boiling point:
374.6±44.0 °C(Predicted)
Density 
1.745
storage temp. 
Inert atmosphere,Room Temperature
pka
3.95±0.10(Predicted)
Appearance
White to off-white Solid
BRN 
141235
CAS DataBase Reference
50907-23-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-41
Safety Statements 
26-39
RIDADR 
UN1759
WGK Germany 
3
HazardClass 
8

MSDS

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5-(4-BROMO-PHENYL)-2H-TETRAZOLE Usage And Synthesis

Synthesis

623-00-7

50907-23-8

The general procedure for the synthesis of 5-(4-bromophenyl)-1H-tetrazole from 4-bromobenzonitrile was as follows: at 85 °C, a tetrabutylammonium fluoride trihydrate (TABF-3H2O) (1.31 g, 5 mmol), 4-bromobenzonitrile (1.82 g, 10 mmol), and trimethylmethylsilylazide (TMSN3) (1.73 g, 15 mmol) The mixture was reacted under vigorous stirring conditions for 18 hours. After completion of the reaction, the reaction mixture was cooled to room temperature, ethyl acetate (EtOAc) was added and washed with 3 x 150 mL hydrochloric acid (HCl). The organic layer was separated and the remaining aqueous phase was further extracted with ethyl acetate. All organic phases were combined, dried with anhydrous magnesium sulfate (MgSO4), filtered and concentrated under reduced pressure to afford the target product 5-(4-bromophenyl)-1H-tetrazole in 97.2% yield. The melting point of the product was 260-261 °C. 1H NMR (400 MHz, DMSO-d6) data: δ 8.19-7.89 (m, 2H), 7.83 (d, J = 8.6 Hz, 2H). 13C NMR (400 MHz, DMSO-d6) data: δ 132.98 (s), 129.36 (s), 125.20 (s) .

References

[1] Journal of the Brazilian Chemical Society, 2012, vol. 23, # 12, p. 2197 - 2203
[2] Tetrahedron Letters, 2014, vol. 55, # 44, p. 6034 - 6038
[3] Synthetic Communications, 2015, vol. 45, # 8, p. 1023 - 1030
[4] Transition Metal Chemistry, 2017, vol. 42, # 8, p. 703 - 710
[5] Angewandte Chemie - International Edition, 2010, vol. 49, # 39, p. 7101 - 7105

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