1H-Benzimidazole-2-carboxylicacid,1-methyl-,methylester(9CI)

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Products Intro: Product Name:methyl 1-methyl-1H-benzo[d]imidazole-2-carboxylate
CAS:2849-92-5
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Products Intro: Product Name:1H-Benzimidazole-2-carboxylicacid,1-methyl-,methylester(9CI)
CAS:2849-92-5
Purity:0.95;0.97;0.98;0.99 Package:mg;g;kg;t Remarks:Reagent grade; Industrial grade
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Products Intro: Product Name:1H-Benzimidazole-2-carboxylicacid,1-methyl-,methylester(9CI)
CAS:2849-92-5
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Products Intro: Product Name:Methyl1-methyl-1H-benzo[d]imidazole-2-carboxylate
CAS:2849-92-5
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Products Intro: Product Name:Methyl 1-methyl-1H-benzo[d]imidazole-2-carboxylate
CAS:2849-92-5
Purity:98% Package:$272.9/25mg;$652.9/100mg;Bulk package Remarks:98%
1H-Benzimidazole-2-carboxylicacid,1-methyl-,methylester(9CI) Basic information
Product Name:1H-Benzimidazole-2-carboxylicacid,1-methyl-,methylester(9CI)
Synonyms:1H-Benzimidazole-2-carboxylicacid,1-methyl-,methylester(9CI);methyl 1-methyl-2-benzimidazolecarboxylate;1-Methyl-1H-benzoimidazole-2-carboxylic acid methyl ester;1H-Benzimidazole-2-carboxylic acid, 1-methyl-, methyl ester;methyl 1-methyl-1H-benzo[d]imidazole-2-carboxylat
CAS:2849-92-5
MF:C10H10N2O2
MW:190.2
EINECS:
Product Categories:BENZIMIDAZOLE
Mol File:2849-92-5.mol
1H-Benzimidazole-2-carboxylicacid,1-methyl-,methylester(9CI) Structure
1H-Benzimidazole-2-carboxylicacid,1-methyl-,methylester(9CI) Chemical Properties
Melting point 88 °C
Boiling point 326.4±25.0 °C(Predicted)
density 1.23±0.1 g/cm3(Predicted)
storage temp. 2-8°C
pka3.51±0.10(Predicted)
AppearanceLight yellow to yellow Solid
Safety Information
MSDS Information
1H-Benzimidazole-2-carboxylicacid,1-methyl-,methylester(9CI) Usage And Synthesis
Synthesis
1H-Benzimidazole-2-carboxylicacid,methylester(9CI)

5805-53-8

Iodomethane

74-88-4

1H-Benzimidazole-2-carboxylicacid,1-methyl-,methylester(9CI)

2849-92-5

To a solution of 1H-benzimidazole-2-carboxylic acid methyl ester (177 mg, 1.0 mmol) in anhydrous N,N-dimethylformamide (DMF, 5 mL) was added sodium hydride (60% dispersed in mineral oil, 62 mg, 1.5 mmol) at 0 °C under nitrogen protection. The reaction mixture was stirred at 0 °C for 0.5 h. After that, iodomethane (284 mg, 2.0 mmol) was slowly added. Subsequently, the reaction mixture was continued to be stirred at room temperature for 4 hours. After completion of the reaction, the mixture was diluted with saturated saline at 0 °C and extracted with ethyl acetate (3 x 20 mL). The combined organic phases were washed sequentially with water (2 x 15 mL) and saturated saline (20 mL), dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure and purified by fast column chromatography to afford methyl 1-methyl-1H-benzimidazole-2-carboxylate (180 mg, 90% yield) as a light yellow solid.ESI-MS (M + 1): 191 (calculated value: C10H10N2O2).

References[1] Patent: WO2011/143365, 2011, A1. Location in patent: Page/Page column 170-171
1H-Benzimidazole-2-carboxylicacid,1-methyl-,methylester(9CI) Preparation Products And Raw materials
Raw materials2-Benzimidazolecarboxylic acid-->1-METHYLBENZIMIDAZOLE-->1H-Benzimidazole-2-carboxylicacid,methylester(9CI)-->Carbon dioxide-->Iodomethane-->Mineral oil-->Sodium hydride-->N,N-Dimethylformamide
Preparation Products1-METHYL-1H-BENZIMIDAZOLE-2-CARBOXYLIC ACID
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