4-METHYL-1H-BENZOIMIDAZOLE

4-METHYL-1H-BENZOIMIDAZOLE Suppliers list
Company Name: Changzhou Xinkai Chemical Co., Ltd.  Gold
Tel: 15051102731
Email: 2455461715@qq.com
Company Name: Beijing HwrkChemical Technology Co., Ltd  
Tel: 89508211 18501085097
Email: sales.bj@hwrkchemical.com
Company Name: BeiJing Hwrk Chemicals Limted  
Tel: 0757-86329057 18934348241
Email: sales4.gd@hwrkchemical.com
Company Name: Jia Xing Isenchem Co.,Ltd  
Tel: 0573-85285100 18627885956
Email: isenchem@163.com
Company Name: Shanghai HuiKe Trading Co., Ltd.  
Tel: 15026939015
Email: michael.liu16@yahoo.com

4-METHYL-1H-BENZOIMIDAZOLE manufacturers

4-METHYL-1H-BENZOIMIDAZOLE Basic information
Product Name:4-METHYL-1H-BENZOIMIDAZOLE
Synonyms:1H-Benzimidazole,4-methyl-(9CI);1H-Benzimidazole, 7-methyl-;4-Methyl-1H-benzo[d]iMidazole/7-Methyl-1H-benzo[d]iMidazole;4-MethylbenziMidazole;7-methyl-1H-Benzimidazole;4-Methyl-1H-1,3-benzodiazole;4-Methyl-1H-benzo[d]iMidazole;7-Methyl-1H-benzo[d]iMidazole
CAS:4887-83-6
MF:C8H8N2
MW:132.16
EINECS:
Product Categories:BENZIMIDAZOLE
Mol File:4887-83-6.mol
4-METHYL-1H-BENZOIMIDAZOLE Structure
4-METHYL-1H-BENZOIMIDAZOLE Chemical Properties
Melting point 140 °C(Solv: ethyl acetate (141-78-6); ligroine (8032-32-4))
Boiling point 363.2±11.0 °C(Predicted)
density 1.186±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka13.15±0.30(Predicted)
AppearanceLight yellow to yellow Solid
Safety Information
HS Code 2933998090
MSDS Information
4-METHYL-1H-BENZOIMIDAZOLE Usage And Synthesis
Synthesis Reference(s)Tetrahedron Letters, 5, p. 2999, 1964 DOI: 10.1002/lipi.19640660210
Synthesis
Triethyl orthoformate

122-51-0

2,3-DIAMINOTOLUENE

2687-25-4

4-METHYL-1H-BENZOIMIDAZOLE

4887-83-6

Example 17: Synthesis of N'-(3,4-dimethoxybenzylidene)-3-(4-methyl-1H-benzo[d]imidazol-1-yl)propanoylhydrazine. [0523] (a) Preparation of 4-methyl-1H-benzo[d]imidazole: 3-methylbenzene-1,2-diamine (400 mg, 3.27 mmol), triethyl orthoformate (0.65 mL, 3.92 mmol) and iodine (83 mg, 0.327 mmol) were mixed in acetonitrile (10 mL) and stirred overnight at room temperature. After completion of the reaction, the reaction mixture was diluted with ethyl acetate and washed with saturated aqueous sodium bicarbonate. The organic layer was separated and dried with anhydrous sodium sulfate. Purification by silica gel column chromatography using ethyl acetate-hexane (0 to 80%) as eluent afforded the target product 4-methyl-1H-benzo[d]imidazole (310 mg, 72% yield).

References[1] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2008, vol. 47, # 7, p. 1154 - 1159
[2] Monatshefte fur Chemie, 2007, vol. 138, # 1, p. 89 - 94
[3] Journal of Heterocyclic Chemistry, 2007, vol. 44, # 6, p. 1509 - 1512
[4] Patent: WO2010/132615, 2010, A1. Location in patent: Page/Page column 113
4-METHYL-1H-BENZOIMIDAZOLE Preparation Products And Raw materials
Raw materials1,1-Dichlorodimethyl ether-->Triethyl orthoformate-->2-Methyl-6-nitroaniline-->Thiourea dioxide-->2,3-DIAMINOTOLUENE-->Acetonitrile-->iodine
Tag:4-METHYL-1H-BENZOIMIDAZOLE(4887-83-6) Related Product Information
1H-BENZIMIDAZOLE, 4-FLUORO- VANOX ZMTI Candesartan 2-Amino-3,4-dimethyl-3H-imidazo[4,5-f]quinoline 2-Azido-3,4,7,8-tetramethyl-3H-imidazo[4,5-f]quinoxaline 2-Azido-3,4,8-trimethyl-3H-imidazo[4,5-f]quinoxaline 2-Amino-3,4-dimethyl-3H-imidazo[4,5-f]quinoline-2-13C 2-AMINO-5-CHLORO-3,4-DIMETHYL-3H-IMIDAZO[4,5-F]QUINOLINE 2-Amino-3,4,8-trimethyl-3H-imidazo[4,5-f]quinoxaline-2-14C 2-Amino-3,4,7,8-tetramethyl-3H-imidazo[4,5-F]quinoxaline 4-METHYL-1H-BENZOIMIDAZOLE 4-(4-METHYL-1 H-BENZOIMIDAZOL-2-YL)-PHENYLAMINE 2-AMINO-3,4,8-TRIMETHYL-3H-IMIDAZO[4,5-F]QUINOXALINE 3,4-Dimethyl-2-nitro-3H-imidazo[4,5-F]quinoline 2-Azido-3,4-dimethylimidazo[4,5-f]quinoline 2-Amino-3,4-dimethyl-3H-imidazo[4,5-f]quinoline-2-14C 4-METHYL-2-PHENYLBENZIMIDAZOLE 2-Amino-3,4,7,8-tetramethyl-3H-imidazo[4,5-f]quinoxaline 2-14C