60367-52-4

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
5-Chloro-2-phenyl-3H-imidazole-4-carbaldehyde is utilized as a building block in the synthesis of pharmaceuticals and agrochemicals. Its unique structure and reactivity allow it to be a key component in the development of new drugs and pesticides.
Used in Medicinal Chemistry and Drug Discovery:
5-Chloro-2-phenyl-3H-imidazole-4-carbaldehyde serves as a valuable intermediate in medicinal chemistry and drug discovery. Its ability to interact with biological targets makes it a promising candidate for the creation of novel compounds with diverse pharmacological properties.
Used in Organic Synthesis:
5-Chloro-2-phenyl-3H-imidazole-4-carbaldehyde is employed as a versatile intermediate in organic synthesis. Its structure enables the synthesis of a wide range of novel compounds with various applications in different industries, including pharmaceuticals, agrochemicals, and other chemical-based sectors.

InChI:InChI=1/C10H7ClN2O/c11-9-8(6-14)12-10(13-9)7-4-2-1-3-5-7/h1-6H,(H,12,13)

Upstream product

• 32683-07-1 N-carboxymethylbenzamidine 

Downstream Products

• 570424-28-1 5-chloro-3-[4-(5,5-dimethyl-[1,3,2]dioxaborinan-2-yl)benzyl]-2-phenyl-3H-imidazole-4-carbaldehyde 
• 1018822-30-4 1-(4-((5-chloro-2-phenyl-1H-imidazol-4-yl)methyl)piperazin-1-yl)-2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)piperidin-2-yl)methoxy)ethanone 
• 1035123-97-7 5-chloro-3-methyl-2-phenyl-3H-imidazole-4-carbaldehyde 
• 1202263-15-7 4-chloro-1-(4-methoxybutyl)-2-phenyl-1H-imidazole-5-carbaldehyde 
• 210824-81-0 4'-(5-Acetyl-4-chloro-2-phenylimidazol-1-ylmethyl)biphenyl-2-sulfonamide 
• 210824-59-2 4'-(4-Chloro-5-formyl-2-phenylimidazol-1-ylmethyl)biphenyl-2-sulfonamide 
• 210824-62-7 4'-(4-Methoxy-5-formyl-2-phenylimidazol-1-ylmethyl)biphenyl-2-sulfon-amide 
• 1202263-17-9 4-chloro-1-(4-methoxybutyl)-2-phenyl-1H-imidazole-5-carboxylic acid 

Relevant academic research and scientific papers

Process for the production of 2-substituted 5-chloroimidazole-4-carbaldehydes

A process for the preparation of 2-substituted 5-chloroimidazole-4-carbaldehydes of the general formula: STR1 in which glycine is reacted with an imido ester of the general formula: STR2 and the resultant intermediate is converted into the product by a Vilsmeier reagent. The 2-substituted 5-chloroimidazole-4-carbaldehydes are valuable intermediates for the preparation of pharmaceuticals or herbicidally active compounds.