13739-49-6

Basic information

• Product Name: 1H-Imidazole, 2,4-dimethyl-5-phenyl-
• CAS NO: 13739-49-6
• Molecular Formula: C11H12N2
• Molecular Weight: 172.23
• Mol File: 13739-49-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1H-Imidazole, 2,4-dimethyl-5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Imidazole, 2,4-dimethyl-5-phenyl-(13739-49-6)
• EPA Substance Registry System: 1H-Imidazole, 2,4-dimethyl-5-phenyl-(13739-49-6)

Safety Data

• Hazardous Substances Data: 13739-49-6(Hazardous Substances Data)

Upstream product

• 98-80-6 phenylboronic acid 
• 930-62-1 2,4-Dimethylimidazole 
• 143-37-3 acetamidine 
• 22596-45-8 2-methyl-2-nitro-3-phenyloxirane 
• 705-60-2 (2-nitroprop-1-enyl)benzene 
• 124-42-5 acetamidine hydrochloride 
• 93-55-0 1-phenyl-propan-1-one 
• 87456-64-2 α-tosyloxypropiophenone 
• 103987-02-6 3,6-dimethyl-5-phenyl-[1,2,4]triazine 
• 64-17-5 ethanol 
• 64-19-7 acetic acid 
• 5650-45-3 2-(morpholin-4-yl)-1-phenylpropan-1-one 
• 75-07-0 acetaldehyde 
• 579-07-7 1-Phenylpropane-1,2-dione 

Relevant articles and documents

FERROPORTIN INHIBITORS AND METHODS OF USE

The subject matter described herein is directed to Ferroportin inhibitor compounds of Formula I and pharmaceutical salts thereof, methods of preparing the compounds, pharmaceutical compositions comprising the compounds and methods of administering the compounds for prophylaxis and/or treatment of diseases caused by a lack of hepcidin or iron metabolism disorders, particularly iron overload states, such as thalassemia, sickle cell disease and hemochromatosis.

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

Hypervalent iodine in synthesis 81: A one-pot procedure for the synthesis of 1H-imidazole derivatives by cyclocondensation of ketones with [Hydroxy(tosyloxy)iodo]benzene and amidines

Tosyloxylation of ketones with [hydroxy(tosyloxy)iodo]benzene (HTIB), followed by treatment with amidines provides a one-pot procedure for the synthesis of 1H-imidazole derivatives with good yields.