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1H-Imidazole, 4,5-diphenyl-1-propyl- is a chemical compound with the molecular formula C18H18N2. It is a derivative of imidazole, a heterocyclic aromatic organic compound containing a benzene ring fused to a diazole ring. The compound is characterized by the presence of two phenyl groups attached to the imidazole ring at positions 4 and 5, and a propyl chain attached to the nitrogen atom at position 1. 1H-Imidazole, 4,5-diphenyl-1-propyl- is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique chemical structure and properties. It is important to note that handling and usage of 1H-Imidazole, 4,5-diphenyl-1-propyl- should be done with caution, as it may have specific safety and health considerations.

1837-56-5

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1837-56-5 Usage

Type of compound

Imidazole derivative

Structure

Contains a 4,5-diphenyl-1-propyl group attached to the imidazole ring

Pharmacological and biological activities

Known for diverse properties, including antifungal, antibacterial, and antiviral

Potential applications

Development of new drugs and pharmaceuticals with specific biological or pharmacological activities

Research status

Additional research is needed to fully understand the potential uses and effects in the field of pharmacology and drug development

Check Digit Verification of cas no

The CAS Registry Mumber 1837-56-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,3 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1837-56:
(6*1)+(5*8)+(4*3)+(3*7)+(2*5)+(1*6)=95
95 % 10 = 5
So 1837-56-5 is a valid CAS Registry Number.

1837-56-5Downstream Products

1837-56-5Relevant academic research and scientific papers

Cycloadditions with Azirines under the Conditions of Photoinduced Electron Transfer: A New Method for the Synthesis of Imidazoles and Heterophanes

Mueller, Felix,Mattay, Jochen

, p. 543 - 550 (2007/10/02)

With the opening of azirine rings under the conditions of photoinduced electron transfer a new synthon for the synthesis of heterocycles is available.The formed 2-azaallenyl radical cation readily reacts with imine to form N-substituted imidazoles in reasonable yields.The synthesis of pyrrolophanes and imidazolophanes from bicyclic azirines is possible as well.With oligocyclic azirines complex heteroaromatic systems and even a porphyrin system can be built up. Key Words: Azirines / Imidazoles / Pyrrolophanes / Electron transfer reaction, photoinduced / 2-Azaallenyl radical cations

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