826-83-5

Basic information

• Product Name: 1H-Imidazole, 4-methyl-5-phenyl-
• CAS NO: 826-83-5
• Molecular Formula: C10H10N2
• Molecular Weight: 158.203
• Mol File: 826-83-5.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 1H-Imidazole, 4-methyl-5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Imidazole, 4-methyl-5-phenyl-(826-83-5)
• EPA Substance Registry System: 1H-Imidazole, 4-methyl-5-phenyl-(826-83-5)

Safety Data

• Hazardous Substances Data: 826-83-5(Hazardous Substances Data)

Usage

Functional Groups

Imidazole and Phenyl

Type of Compound

Heterocyclic Aromatic Compound

Biological Activities

Anti-fungal and Anti-bacterial Properties

Applications

Building Block in Synthesis of Pharmaceutical Drugs and Agrochemicals

Use as a Ligand

Coordination Chemistry

Production

Dyes

Versatility

Wide Range of Applications in Pharmaceutical, Agricultural, and Chemical Industries

Upstream product

• 50-00-0 formaldehyd 
• 19347-08-1 acetic acid 1-methyl-2-oxo-2-phenyl-ethyl ester 
• 579-07-7 1-Phenylpropane-1,2-dione 
• 93-55-0 1-phenyl-propan-1-one 
• 77287-34-4 formamide 
• 2114-00-3 2-bromo-1-phenyl-1-propanone 
• 3473-63-0 formamidine acetic acid 
• 22596-45-8 2-methyl-2-nitro-3-phenyloxirane 
• 463-52-5 formamidine 
• 81225-10-7 6-Chloro-2-methyl-3-phenylpyrazine 
• 83505-93-5 2-azido-6-methyl-5-phenylpyrazine 
• 83505-81-1 1-cyano-5-methyl-4-phenylimidazole 
• 822-36-6 4-methyl-1H-imidazole 
• 98-80-6 phenylboronic acid 

Downstream Products

• 117044-29-8 4-cyclohexyl-5-methyl-1⁽³⁾H-imidazole 
• 141815-91-0 1-(3-chloropropyl)-5-methyl-4-phenylimidazole 
• 1026004-93-2 3-(5-methyl-4-phenyl-1H-imidazol-1-yl)propionaldehyde diethyl acetal 
• 148726-36-7 3-<2-hydroxy-3-(5-methyl-4-phenyl-1H-imidazol-1-yl)propoxy>-2-nitrotoluene 
• 62576-11-8 1,4-dimethyl-5-phenyl-1H-imidazole 
• 75815-10-0 5-methyl-4-(4-nitrophenyl)imidazole 
• 141816-06-0 5-methyl-4-phenyl-1-(3-propylthio)imidazole 
• 149156-09-2 N-<2-amino>-6-(dimethylamino)phenyl>-N'-pentylurea 
• 141816-09-3 3-(dimethylamino)-2-nitro-N-benzyl-N-<3-(5-methyl-4-phenyl-1H-imidazol-1-yl)propyl>aniline 
• 141816-08-2 3-chloro-2-nitro-N-benzyl-N-<3-(5-methyl-4-phenyl-1H-imidazol-1-yl)propyl>aniline 

Relevant articles and documents

Novel synthesis of divergent aryl imidazoles from ketones involving copper-catalyzed α-amination and oxidative C-C bond cleavage

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Highly efficient and eco-friendly protocol to functionalized imidazoles via ring-opening of α-nitro epoxides

A simple and direct synthesis of functionalized imidazoles from α-nitro-epoxides and amidines was developed. This reaction could proceed smoothly in a highly efficient and eco-friendly manner in moderate to excellent yields. A plausible mechanism has also

Synthesis of 5-arylhistidines via a Suzuki-Miyaura cross-coupling

Microwave irradiation efficiently promoted the Suzuki-Miyaura reaction of a 5-bromohistidine with various arylboronic acids in the presence of a palladium catalyst. This methodology allowed the synthesis of histidines substituted at position 5 of the imid