(1H-Benzoimidazol-2-yl)-acetic acid

(1H-Benzoimidazol-2-yl)-acetic acid Suppliers list
Company Name: Wuhan Chemwish Technology Co., Ltd  
Tel: 86-027-67849912
Email: sales@chemwish.com
Company Name: Adamas Reagent, Ltd.  
Tel: 400-6009262 15618770481
Email: yhx@titansci.com
Company Name: Nanjing Chemlin Chemical Co., Ltd  
Tel: 025-83697070 13770331960
Email: info@chemlin.com.cn
Company Name: Chemsky(shanghai)International Co.,Ltd.  
Tel: 021-50135380
Email: shchemsky@sina.com
Company Name: China Langchem Inc.  
Tel: 0086-21-58956006
Email:

(1H-Benzoimidazol-2-yl)-acetic acid manufacturers

(1H-Benzoimidazol-2-yl)-acetic acid Basic information
Product Name:(1H-Benzoimidazol-2-yl)-acetic acid
Synonyms:CHEMBRDG-BB 4400292;IFLAB-BB F1727-0259;AKOS BBS-00002502;RARECHEM AK ML 0141;1H-Benzimidazole-2-aceticacid(9CI);1H-Benzimidazole-2-acetic acid;1H-benzimidazol-2-ylacetic acid(SALTDATA: FREE);2-(1H-1H-benzo[d]iMidazol-2-yl)-acetic acid
CAS:13570-08-6
MF:C9H8N2O2
MW:176.17
EINECS:
Product Categories:BENZIMIDAZOLE;Carboxylic Acids;Imidazoles & Benzimidazoles;Carboxylic Acids;Imidazoles & Benzimidazoles
Mol File:13570-08-6.mol
(1H-Benzoimidazol-2-yl)-acetic acid Structure
(1H-Benzoimidazol-2-yl)-acetic acid Chemical Properties
Melting point 116 °C
Boiling point 498.3±28.0 °C(Predicted)
density 1.437±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka1.54±0.30(Predicted)
AppearanceLight yellow to light brown Solid
Safety Information
Hazard Codes Xi
HazardClass IRRITANT
MSDS Information
(1H-Benzoimidazol-2-yl)-acetic acid Usage And Synthesis
Uses(1h-Benzoimidazol-2-yl)-acetic Acid is a useful intermediate for the synthesis of benzisothiazole/benzimidazole derivatives with acidic groups that exhibits numerous pharmacological properties.
Synthesis Reference(s)Journal of Medicinal Chemistry, 36, p. 1746, 1993 DOI: 10.1021/jm00064a008
Synthesis
2-(Cyanomethyl)benzimidazole

4414-88-4

(1H-BENZOIMIDAZOL-2-YL)-ACETIC ACID

13570-08-6

General procedure for the synthesis of benzimidazole-2-acetic acid from 2-cyanomethylbenzimidazole: A mixture of 1 g of 2-cyanomethylbenzimidazole (3a-b) with 2 ml of 37% aqueous hydrochloric acid in the presence of 1 ml of benzenesulphonic acid was heated and stirred under reflux conditions for 4-5 hours. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was cooled to room temperature and extracted with ether (3 x 30 ml), followed by removal of solvent by distillation under reduced pressure to afford the target products benzimidazole-2-acetic acid (4a-b). 4.3.1. 1H-benzimidazole-2-acetic acid (4a, C9H8N2O2) was a green solid, hygroscopic, with a yield of 81% and a melting point of 240-242 °C; TLC Rf value of 0.42 [unfolding reagent ratio of toluene: ethyl acetate: formic acid (5:4:1)]; IR spectra (KBr, cm^-1 ): 3624 (O-H telescoping vibration) 3230 (N-H stretching vibration), 1722 (C=O stretching vibration); 1H NMR (300MHz, DMSO-d6) δ (ppm): 3.64 (single peak, 2H, CH2COOH), 7.58 (double peaks, 2H, J=7.5,0.9Hz, H-5,6 on benzimidazole ring), 7.92 (double peaks, 2H, J=7.5 Hz, H-4,7 on the benzimidazole ring), 10.59 (broad peak, 1H, COOH), 12.03 (broad peak, 1H, NH).13C NMR (75 MHz, DMSO-d6) δ (ppm): 164.20, 152.20, 131.95, 128.32, 122.50, 48.40. Calculated values for elemental analysis (%) : C, 61.36; H, 4.58; N, 15.90; measured values (%): C, 61.33; H, 4.56; N, 15.92.

References[1] Patent: US5792768, 1998, A
[2] Farmaco, 2002, vol. 57, # 5, p. 363 - 367
[3] European Journal of Medicinal Chemistry, 2017, vol. 126, p. 853 - 869
[4] Journal of Medicinal Chemistry, 1993, vol. 36, # 12, p. 1746 - 1753
[5] Patent: WO2017/68089, 2017, A2. Location in patent: Page/Page column 243
(1H-Benzoimidazol-2-yl)-acetic acid Preparation Products And Raw materials
Raw materials2-(Cyanomethyl)benzimidazole-->Benzenesulfonic acid-->Hydrochloric acid
Preparation Products1H-Benzimidazole-2-aceticacid,methylester(9CI)
Tag:(1H-Benzoimidazol-2-yl)-acetic acid(13570-08-6) Related Product Information
Benzomorpholine 2-(Benzofuran-2-yl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione, 2-Benzofuranboronic acid MIDA ester Benzimidazole-5,6-dicarboxylic acid 2-Aminobenzo[b]thiophene 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzo[d]thiazole Benzothiazole-2-acetonitrile 6-BENZOFURANAMINE 1-benzofuran-3-carboxylic acid Methyl benzo[b]thiophene-2-carboxylate 4-Benzofurancarboxylicacidmethylester Benzofuran-3-boronic acid 2-Cyanobenzofuran Coumarin 30 DISPERSE YELLOW 82 (2-METHYL-BENZOIMIDAZOL-1-YL)ACETIC ACID 2-Benzimidazolepropionic acid (1H-Benzoimidazol-2-yl)-acetic acid ethyl ester 2-Chloro-5-methoxybenzimidazole