1-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE

1-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE
  • CAS No.:25371-96-4
Other grades of this product :
1-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE Basic information
Product Name:1-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE
Synonyms:I-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE;1-(ALPHA,ALPHA,ALPHA-TRIFLUORO-O-TOLYL)-IMIDAZOLE;1-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE;1-[2-(TRIFLUOROMETHYL)PHENYL]-1H-IMIDAZOLE;TRIM;1-[2-(Trifluoromethyl)phenyl]-1H-imidazole 98%;1-[2-(Trifluoromethyl)phenyl]-1H-imidazole98%;1-(2-Trifluoromethylphenyl)imidazole, 98+%
CAS:25371-96-4
MF:C10H7F3N2
MW:212.17
EINECS:636-734-9
Product Categories:Imidazol&Benzimidazole
Mol File:25371-96-4.mol
1-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE Chemical Properties
Melting point 43 °C
Boiling point 75°C 0,02mm
density 1.3253 (estimate)
Fp 75°C/0.025mm
storage temp. 2-8°C
solubility Soluble in DMSO (up to 10 mg/ml) or in Ethanol (up to 20 mg/ml).
form White solid.
pka4.96±0.10(Predicted)
color White
Sensitive Light Sensitive
BRN 3955637
Stability:Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 3 months.
CAS DataBase Reference25371-96-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
Hazard Note Irritant
HazardClass IRRITANT, LIGHT SENSITIVE
HS Code 29339900
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
1-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE Usage And Synthesis
DescriptionTRIM (25371-96-4) is a potent inhibitor of neuronal and inducible nitric oxide synthases, (IC50?= 28.2 and 27.0 μM respectively). Inhibits endothelial NOS with lower potency (IC50 = 1057.5 μM).1?TRIM displays antinociceptive activity?in vivo.2
UsesTRIM is a potent inhibitor of neuronal nitric oxide synthase in vitro, in animal models.
Biological ActivityA potent inhibitor of neuronal and inducible NO synthases, with much lower affinity for the endothelial isoform (displays IC 50 values of 28.2, 27.0 and 1057.5 μ M respectively). Antinociceptive in vivo .
Biochem/physiol ActionsPotent nitric oxide synthase inhibitor. Because of the putative involvement of nitric oxide in depression and stress syndromes, TRIM was studied for its antidepressant effects, and found to reduce manifestations of stress in an animal model as well as fluoxetine.
References1) Handy?et al. (1995), The antinociceptive effect of 1-(2-trifluoromethylphenyl)imidazole (TRIM), a potent inhibitor of neuronal nitric oxide synthase in vitro, in the mouse; Br. J. Pharmacol.,?116?2349 2) Handy?et al. (1996),?Inhibition of nitric oxide synthase by 1-(2-trifluoromethylphenyl) imidazole (TRIM) in vitro: antinociceptive and cardiovascular effects; Br. J. Pharmacol.,?119?423
1-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE Preparation Products And Raw materials

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