705-09-9 | 2-Difluoromethyl-1H-benzoimidazole

CAS:705-09-9 | 2-Difluoromethyl-1H-benzoimidazole,Description

2-(Difluoromethyl)-1H-benzimidazole is a chemical compound. However, there is limited information available about this specific compound¹².

Synthesis Analysis

The synthesis of difluoromethyl compounds has been a topic of interest in recent years³⁴. However, the specific synthesis process for 2-(Difluoromethyl)-1H-benzimidazole is not readily available in the sources I found.
 

Molecular Structure Analysis

The molecular structure of a compound can provide insights into its properties and potential applications⁵⁶⁷. However, the specific molecular structure analysis for 2-(Difluoromethyl)-1H-benzimidazole is not detailed in the sources I found.
 

Chemical Reactions Analysis

Chemical reactions involving difluoromethyl compounds have been studied⁸⁹. However, specific chemical reactions involving 2-(Difluoromethyl)-1H-benzimidazole are not detailed in the sources I found.
 

Physical And Chemical Properties Analysis

The physical and chemical properties of a compound can provide insights into its potential applications¹²¹³. However, the specific physical and chemical properties of 2-(Difluoromethyl)-1H-benzimidazole are not detailed in the sources I found.
 

Scientific Research Applications

• Scientific Field : Organic Chemistry 
• Summary of the Application : Difluoromethylation is a process that involves the formation of X–CF2H bonds, where X can be C (sp), C (sp2), C (sp3), O, N, or S. This process is of prime importance due to its applicability in functionalizing diverse fluorine-containing heterocycles, which are the core moieties of various biologically and pharmacologically active ingredients.
• Methods of Application or Experimental Procedures : The difluoromethylation process has benefited from the invention of multiple difluoromethylation reagents. The last decade has witnessed an upsurge of metal-based methods that can transfer CF2H to C (sp2) sites both in stoichiometric and catalytic mode. Difluoromethylation of C (sp2)–H bond has also been accomplished through Minisci-type radical chemistry, a strategy best applied to heteroaromatics.
• Results or Outcomes : These advances have streamlined access to molecules of pharmaceutical relevance, and generated interest for process chemistry. The construction of difluoromethyl substituted scaffolds has been a highly intriguing research topic, and substantial progress has been made in the past decades.
• Scientific Field : Organic Chemistry 
• Summary of the Application : Difluoromethylation is a process that involves the formation of X–CF2H bonds, where X can be C (sp), C (sp2), C (sp3), O, N, or S. This process is of prime importance due to its applicability in functionalizing diverse fluorine-containing heterocycles, which are the core moieties of various biologically and pharmacologically active ingredients.
• Methods of Application or Experimental Procedures : The difluoromethylation process has benefited from the invention of multiple difluoromethylation reagents. The last decade has witnessed an upsurge of metal-based methods that can transfer CF2H to C (sp2) sites both in stoichiometric and catalytic mode. Difluoromethylation of C (sp2)–H bond has also been accomplished through Minisci-type radical chemistry, a strategy best applied to heteroaromatics.
• Results or Outcomes : These advances have streamlined access to molecules of pharmaceutical relevance, and generated interest for process chemistry. The construction of difluoromethyl substituted scaffolds has been a highly intriguing research topic, and substantial progress has been made in the past decades.
• Scientific Field : Organic Chemistry 
• Summary of the Application : Difluoromethylation is a process that involves the formation of X–CF2H bonds, where X can be C (sp), C (sp2), C (sp3), O, N, or S. This process is of prime importance due to its applicability in functionalizing diverse fluorine-containing heterocycles, which are the core moieties of various biologically and pharmacologically active ingredients.
• Methods of Application or Experimental Procedures : The difluoromethylation process has benefited from the invention of multiple difluoromethylation reagents. The last decade has witnessed an upsurge of metal-based methods that can transfer CF2H to C (sp2) sites both in stoichiometric and catalytic mode. Difluoromethylation of C (sp2)–H bond has also been accomplished through Minisci-type radical chemistry, a strategy best applied to heteroaromatics.
• Results or Outcomes : These advances have streamlined access to molecules of pharmaceutical relevance, and generated interest for process chemistry. The construction of difluoromethyl substituted scaffolds has been a highly intriguing research topic, and substantial progress has been made in the past decades.

Safety And Hazards

Understanding the safety and hazards of a compound is crucial for its handling and use¹⁴¹⁵. However, the specific safety and hazards associated with 2-(Difluoromethyl)-1H-benzimidazole are not detailed in the sources I found.

Future Directions

Research into difluoromethyl compounds continues to be a topic of interest, with potential applications in various fields¹⁶¹⁷. However, the specific future directions for research into 2-(Difluoromethyl)-1H-benzimidazole are not detailed in the sources I found.

Please note that while I strive to provide accurate and up-to-date information, the details provided should be verified with a reliable source or expert in the field. The information provided is based on the sources I found and may not be comprehensive or entirely accurate.

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