Basic information Uses Safety Supplier Related

4-TRIFLUOROMETHYL-BENZAMIDINE HCL

Basic information Uses Safety Supplier Related

4-TRIFLUOROMETHYL-BENZAMIDINE HCL Basic information

Product Name:
4-TRIFLUOROMETHYL-BENZAMIDINE HCL
Synonyms:
  • 4-TRIFLUOROMETHYL-BENZAMIDINE HCL
  • 4-TRIFLUOROMETHYL-BENZAMIDINE HYDROCHLORIDE
  • 4-Trifluoromethylbenzamidinehydrochloridel
  • 4-(Trifluoromethyl)benzenecarboximidamide hydrochloride
  • 4-TrifluoroMethyl-benzanidibe HCL
  • 4-(TrifluoroMethyl)benzenecarboxiMidaMide hydrochloride (1:1)
  • 4-(Trifluoromethyl)benzene-1-carboximidamide hydrochloride
  • 4-TRIFLUOROMETHYL-BENZAMIDINE HCL ISO 9001:2015 REACH
CAS:
38980-96-0
MF:
C8H8ClF3N2
MW:
224.61
Product Categories:
  • pharmacetical
Mol File:
38980-96-0.mol
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4-TRIFLUOROMETHYL-BENZAMIDINE HCL Chemical Properties

Melting point:
158-161℃
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
color 
White to Almost white
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-43
Safety Statements 
26-37/39-36/37
HS Code 
2925290090
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4-TRIFLUOROMETHYL-BENZAMIDINE HCL Usage And Synthesis

Uses

4-Trifluoromethylbenzamide hydrochloride is used as a pharmaceutical synthesis intermediate.

Synthesis

455-18-5

38980-96-0

4-(Trifluoromethyl)benzonitrile (15g, Avocado 14514) was used as raw material, which was dissolved in anhydrous methanol (90 ml) and sodium methanolate (0.50 g) was added. The reaction mixture was stirred at room temperature for 4 days. Subsequently, ammonium chloride (4.7 g) was added to the reaction system and stirring was continued for 24 hours. Upon completion of the reaction, the solvent was removed by rotary evaporator and the white solid residue obtained was ground with ether, filtered and dried to afford the target product 4-(trifluoromethyl)benzamidine hydrochloride as a white solid (14.2 g, 72% yield). Mass spectrometry analysis showed a molecular ion peak of 188 [M]+.

References

[1] Patent: US2003/69276, 2003, A1
[2] Journal of the American Chemical Society, 1985, vol. 107, # 9, p. 2743 - 2748
[3] Journal of Medicinal Chemistry, 1990, vol. 33, # 4, p. 1230 - 1241
[4] Patent: US6121202, 2000, A
[5] Patent: US2012/165343, 2012, A1. Location in patent: Page/Page column 55

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