Identification | Back Directory | [Name]
1H-BENZIMIDAZOLE-2-ETHANAMINE DIHYDROCHLORIDE, 97 | [CAS]
4499-07-4 | [Synonyms]
1H-Benzimidazole-2-ethanamine 2-(2-Aminoethyl)benzimidazole dihydrochloride 2-(2-AMinoethyl)benzoiMidazole Dihydrochloride 2-(2-AMinoethyl)benziMidazole dihydrochloride 97% 1H-BENZIMIDAZOLE-2-ETHANAMINE DIHYDROCHLORIDE, 97 2-(1H-Benzoimidazol-2-yl)ethylaminedihydrochloride 2-(1H-benzo[d]iMidazol-2-yl)ethanaMine hydrochloride 1H-BenziMidazole-ethanaMine dihydrochloride, HPLC 97% 2-(1H-Benzo[d]iMidazol-2-yl)ethanaMine dihydrochloride 1H-Benzimidazole-2-ethanamine, 2-(1H-Benzimidazol-2-yl)ethylamine | [Molecular Formula]
C9H13Cl2N3 | [MDL Number]
MFCD01325081 | [MOL File]
4499-07-4.mol | [Molecular Weight]
234.126 |
Chemical Properties | Back Directory | [Appearance]
White to slightly grey crystalline powder | [Melting point ]
235 °C | [storage temp. ]
Inert atmosphere,Room Temperature | [InChIKey]
LKFGBWROFLZYQJ-UHFFFAOYSA-N | [CAS DataBase Reference]
4499-07-4 |
Hazard Information | Back Directory | [Chemical Properties]
White to slightly grey crystalline powder | [Synthesis]
General procedure for the synthesis of 1H-benzimidazole-2-ethylamine dihydrochloride from the compound (CAS:189560-91-6): compound 3 (3 g) was dissolved in 3N hydrochloric acid/ethyl acetate mixed solvent (50 mL/25 mL) and the reaction was stirred overnight at room temperature. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure and dried under high vacuum to afford compound 4 as a pink solid (2.4 g) in over 95% yield. Analyzed by liquid chromatography-mass spectrometry (LC/MS), the molecular ion peak (M+1) m/z of 162.4 was detected with a retention time of 0.62 min. | [References]
[1] Patent: WO2005/42497, 2005, A2. Location in patent: Page/Page column 221 |
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