Basic information Safety Supplier Related

4-Bromobenzamidine hydrochloride

Basic information Safety Supplier Related

4-Bromobenzamidine hydrochloride Basic information

Product Name:
4-Bromobenzamidine hydrochloride
Synonyms:
  • 4-Bromo-benzamidine hydrochloride ,99%
  • 4-broMobenzene-1-carboxiMidaMide hydrochloride
  • 4-bromobenzimidamide hydrochloride
  • 4-Bromobenzimidamide, HCl
  • 4-Bromobenzamidine Hydrochloride Hydrate
  • Halogenobenzamidine hydrochloride
  • 4-broMobenzaMidine hydrogen chloride
  • 4-BROMO-BENZAMIDINE HYDROCHLORIDE
CAS:
55368-42-8
MF:
C7H8BrClN2
MW:
235.51
Product Categories:
  • Phenyls & Phenyl-Het
  • Phenyls & Phenyl-Het
  • blocks
  • Bromides
  • BuildingBlocks
  • Carboxes
Mol File:
55368-42-8.mol
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4-Bromobenzamidine hydrochloride Chemical Properties

Melting point:
269-272℃ ()
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
soluble in Methanol
form 
Crystalline Solid
color 
White
InChI
InChI=1S/C7H7BrN2.ClH/c8-6-3-1-5(2-4-6)7(9)10;/h1-4H,(H3,9,10);1H
InChIKey
IMTHEBSPHHMJOJ-UHFFFAOYSA-N
SMILES
C(N)(=N)C1=CC=C(Br)C=C1.[H]Cl
CAS DataBase Reference
55368-42-8
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HS Code 
29252900
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4-Bromobenzamidine hydrochloride Usage And Synthesis

Chemical Properties

White solid

Uses

4-Bromobenzimidamide, HCl

Synthesis

623-00-7

55368-42-8

The general procedure for the synthesis of 4-bromobenzamidine hydrochloride from 4-bromobenzonitrile was as follows: hydrogen chloride gas was passed into a mixture of chloroform (300 mL) and ethanol (100 mL) containing 4-bromobenzonitrile (18.2 g) at -65 °C for 35 min. Subsequently, the reaction system was slowly warmed to room temperature and stirred continuously at that temperature overnight. Upon completion of the reaction, the solvent was removed by vacuum evaporation and the resulting residue was redissolved in ethanol (400 mL). Ammonium carbonate (48.0 g) was added to this solution and the reaction mixture was stirred at room temperature for 20 hours. At the end of the reaction, water (300 mL) was added and the ethanol was removed by vacuum concentration. The resulting precipitate was collected by filtration, washed with water and dried under vacuum to afford the target product 4-bromobenzamidine hydrochloride (22.9 g, 97% yield) as a white solid. The product was detected by 1H NMR (DMSO-d6), showing δ 2.55-4.60 (2H, broad peak), 6.30-8.90 (6H, multiple peaks); FAB-MS showed m/z 199,201 [(M + H)+].

References

[1] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 7, p. 2369 - 2375
[2] Bioorganic and Medicinal Chemistry, 2017, vol. 25, # 23, p. 6218 - 6223
[3] Magnetic Resonance in Chemistry, 1987, vol. 25, p. 923 - 927
[4] Physical Chemistry Chemical Physics, 2004, vol. 6, # 4, p. 756 - 765
[5] Tetrahedron Letters, 2018, vol. 59, # 4, p. 361 - 364

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