Basic information Safety Supplier Related

2-(Trifluoromethyl)benzimidazole

Basic information Safety Supplier Related

2-(Trifluoromethyl)benzimidazole Basic information

Product Name:
2-(Trifluoromethyl)benzimidazole
Synonyms:
  • 2-(TRIFLUOROMETHYL)-1H-BENZIMIDAZOLE
  • 2-(TRIFLUOROMETHYL)-1H-BENZO[D]IMIDAZOLE
  • 2-(TRIFLUOROMETHYL)BENZIMIDAZOLE
  • 2-(trifluoromethyl)-1h-benzimidazol
  • 2-trifluoromethyl-benzimidazol
  • RARECHEM AQ NN 0072
  • 3-TRIFLUOROMETHYL BENZIMIDAZOLE
  • 1H-Benzimidazole,2-(trifluoromethyl)-(9CI)
CAS:
312-73-2
MF:
C8H5F3N2
MW:
186.13
Product Categories:
  • BENZIMIDAZOLE
  • Imidazol&Benzimidazole
  • Benzimidazoles
  • Building Blocks
  • Heterocyclic Building Blocks
Mol File:
312-73-2.mol
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2-(Trifluoromethyl)benzimidazole Chemical Properties

Melting point:
208-211 °C(lit.)
Boiling point:
262.8±40.0 °C(Predicted)
Density 
1.3658 (estimate)
storage temp. 
Inert atmosphere,Room Temperature
pka
9.25±0.10(Predicted)
Appearance
Light brown to off-white Solid
Water Solubility 
PRACTICALLY INSOLUBLE
InChI
InChI=1S/C8H5F3N2/c9-8(10,11)7-12-5-3-1-2-4-6(5)13-7/h1-4H,(H,12,13)
InChIKey
MXFMPTXDHSDMTI-UHFFFAOYSA-N
SMILES
C1(C(F)(F)F)NC2=CC=CC=C2N=1
CAS DataBase Reference
312-73-2(CAS DataBase Reference)
NIST Chemistry Reference
2-Trifluoromethylbenzimidazole(312-73-2)
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Safety Information

Hazard Codes 
T,Xi
Risk Statements 
23/24/25-36/37/38
Safety Statements 
22-26-36/37/39-45-28A
RIDADR 
UN 2811 6.1/PG 2
WGK Germany 
3
RTECS 
DE1576000
HazardClass 
6.1(a)
PackingGroup 
II
HS Code 
29332900

MSDS

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2-(Trifluoromethyl)benzimidazole Usage And Synthesis

Chemical Properties

light grey fine powder

Uses

Agricultural chemical.

Hazard

A poison by ingestion.

Synthesis

O-phenylenediamine was dissolved in a 1:1 mixture of methanol and water, trifluoroacetic acid was added, and the reaction was carried out at 50?? for . 2 hours; after cooling to room temperature, concentrated under reduced pressure to remove methanol, the remaining aqueous phase was added to an aqueous sodium hydroxide solution, ethyl acetate was added to extract twice, the organic layers after extraction were combined, and the organic phases were washed with purified water, saturated saline, dried with anhydrous magnesium sulfate, pumped and filtered, spun-dried under reduced pressure to remove the organic solvent, and the residue was recrystallized with ethanol and water, to obtain the product 2-(trifluoromethyl)benzimidazole.

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