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ChemicalBook > Product Catalog >Organic Chemistry >Carboxylic acids and derivatives >1H-Benzimidazole-4-carboxylic acid

1H-Benzimidazole-4-carboxylic acid

1H-Benzimidazole-4-carboxylic acid Suppliers list
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Products Intro: Product Name:1H-BENZOIMIDAZOLE-4-CARBOXYLIC ACID
CAS:46006-36-4
Purity:98% HPLC Package:5MG;10MG;50MG;100MG,1G,5G
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Products Intro: Product Name:1H-Benzimidazole-4-carboxylic Acid
CAS:46006-36-4
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Products Intro: Product Name:1H-Benzimidazole-7-carboxylic acid
CAS:46006-36-4
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1H-Benzimidazole-4-carboxylic acid manufacturers

1H-Benzimidazole-4-carboxylic acid Basic information
Product Name:1H-Benzimidazole-4-carboxylic acid
Synonyms:Benzimidazole-4-carboxylicacid;1H-Benzimidazole-4-carboxylic acid 97%;1H-Benzimidazole-4-carboxylicacid(9CI);4-Benzimidazolecarboxylic acid;4-Carboxy-1H-benzimidazole;1H-benzo[d]iMidazole-7-carboxylic acid;1H-1,3-benzodiazole-4-carboxylic acid;1H-benzo[d]imidazol-7-carboxylic acid
CAS:46006-36-4
MF:C8H6N2O2
MW:162.15
EINECS:
Product Categories:Benzoimidazole;Building Blocks;BENZIMIDAZOLE;pharmacetical;Carboxylic Acids;Imidazoles & Benzimidazoles;Carboxylic Acids;Imidazoles & Benzimidazoles
Mol File:46006-36-4.mol
1H-Benzimidazole-4-carboxylic acid Structure
1H-Benzimidazole-4-carboxylic acid Chemical Properties
Melting point >300 °C
Boiling point 542.5±23.0 °C(Predicted)
density 1.506±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka0.17±0.10(Predicted)
AppearanceOff-white to light brown Solid
Safety Information
Hazard Codes Xi,N
Risk Statements 36-51
Safety Statements 53-26-61
RIDADR UN 3077 9 / PGIII
HazardClass IRRITANT
HS Code 29339980
MSDS Information
1H-Benzimidazole-4-carboxylic acid Usage And Synthesis
Synthesis
Formic acid

64-18-6

2,3-Diaminobenzoic acid

603-81-6

1H-Benzimidazole-4-carboxylic acid

46006-36-4

To a 4M hydrochloric acid (20 mL) solution of formic acid (0.75 mL, 20.0 mmol) was added 2,3-diaminobenzoic acid (1.00 g, 6.6 mmol). The reaction mixture was heated at reflux temperature for 2 h and subsequently cooled to room temperature. The resulting pink precipitate was separated by filtration and dissolved in hot methanol. Decolorization was carried out by adding activated carbon and stirring for 10 min. The suspension was filtered and the solvent was evaporated under reduced pressure to afford benzimidazole-7-carboxylic acid (0.542 g, 51% yield) as white crystals with a melting point of 266-268 °C. The structure of the product was analyzed by 1H NMR (300 MHz, DMSO-d6) δ 9.64 (s, 1H), 8.11 (dd, J = 8.2, 0.9 Hz, 1H), 8.07 (dd, J = 7.6, 0.9 Hz, 1H), 7.65 (dd, J = 8.2, 7.6 Hz, 1H) and 13C NMR (75 MHz, DMSO-d6 ) δ 265.2, 142.0, 132.3, 129.3, 127.6, 125.6, 119.7, 117.6 confirmed.

References[1] Journal of Medicinal Chemistry, 2000, vol. 43, # 22, p. 4084 - 4097
[2] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 14, p. 3933 - 3937
[3] Chemische Berichte, 1901, vol. 34, p. 905
[4] Patent: WO2018/42362, 2018, A1. Location in patent: Page/Page column 50
Tag:1H-Benzimidazole-4-carboxylic acid(46006-36-4) Related Product Information
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