5-METHOXYBENZIMIDAZOLE

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5-METHOXYBENZIMIDAZOLE Basic information
Product Name:5-METHOXYBENZIMIDAZOLE
Synonyms:5-Methoxy-1H-benzoiMidazole;5-Methoxy-1H-benzo[d]iMidazole;5-Methoxybenzimidazole 97%;5-METHOXYBENZIMIDAZOLE;BUTTPARK 146\15-76;5-Methoxybenzimidazole,99%;1H-Benzimidazole,5-methoxy-(9CI);5-Methoxybenzimidazole,97%
CAS:4887-80-3
MF:C8H8N2O
MW:148.16
EINECS:225-502-9
Product Categories:BENZIMIDAZOLE;pharmacetical;Imidazol&Benzimidazole;Benzimidazoles;Building Blocks;Heterocyclic Building Blocks
Mol File:4887-80-3.mol
5-METHOXYBENZIMIDAZOLE Structure
5-METHOXYBENZIMIDAZOLE Chemical Properties
Melting point 121-126 °C (lit.)
Boiling point 190-195 °C(Press: 0.03 Torr)
density 1.244±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form solid
pka13.12±0.10(Predicted)
color Light brown to brown
InChIInChI=1S/C8H8N2O/c1-11-6-2-3-7-8(4-6)10-5-9-7/h2-5H,1H3,(H,9,10)
InChIKeyILMHAGCURJPNRZ-UHFFFAOYSA-N
SMILESC1NC2=CC(OC)=CC=C2N=1
CAS DataBase Reference4887-80-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-20/21/22
Safety Statements 26-36-24/25
WGK Germany 3
HS Code 29332990
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
5-METHOXYBENZIMIDAZOLE Usage And Synthesis
Chemical PropertiesWhite to brown powder
Uses6-Methoxy-1H-benzimidazole has been studied for its anti-proliferative activity, and a preliminary in vivo toxicity study against a panel of non-small cell lung cancer cell lines.
Synthesis
1H-Benzimidazole, 5-methoxy-1-(phenylmethyl)-

22019-71-2

5-METHOXYBENZIMIDAZOLE

4887-80-3

To a 16 mL reaction flask equipped with a PTFE/silicone septum and a nitrogen bubbler was added N-benzylbenzimidazole (208.1 mg, 1.0 mmol), dried Pd/C catalyst (10 wt%, 20 mg) and THF (5 mL). Triethylsilane (320 μL, 2.0 mmol) was added dropwise to the mixture under nitrogen protection, followed by continuous stirring at room temperature for 14 hours. After completion of the reaction, the reaction mixture was filtered through a 0.45 μm PTFE syringe filter and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (eluent: 0 to 10% methanol/dichloromethane gradient) to afford 5-methoxybenzimidazole as a colorless solid (117.6 mg, 0.996 mmol, 99% yield). It is worth noting that the reaction typically suffers from an induction period of 5 to 30 min, which can be observed by the release of gas from the reaction mixture (i.e., the bubbling phenomenon). The use of a dry Pd/C catalyst is critical to the success of the reaction, and wet Pd/C may result in a significant decrease in yield or inability of the reaction to proceed.

References[1] Tetrahedron Letters, 2015, vol. 56, # 21, p. 2688 - 2690
5-METHOXYBENZIMIDAZOLE Preparation Products And Raw materials
Raw materialsEthanol-->Hydrochloric acid-->Ethyl acetate-->Acetic acid-->Nitric acid-->Potassium hydroxide-->Acetic anhydride-->Palladium-->Formic acid-->p-Anisidine
Tag:5-METHOXYBENZIMIDAZOLE(4887-80-3) Related Product Information
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