25699-96-1

Basic information

• Product Name: Ethanone, 1-[2-(1H-pyrazol-1-yl)phenyl]-
• CAS NO: 25699-96-1
• Molecular Formula: C11H10N2O
• Molecular Weight: 186.213
• Mol File: 25699-96-1.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[2-(1H-pyrazol-1-yl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[2-(1H-pyrazol-1-yl)phenyl]-(25699-96-1)
• EPA Substance Registry System: Ethanone, 1-[2-(1H-pyrazol-1-yl)phenyl]-(25699-96-1)

Safety Data

• Hazardous Substances Data: 25699-96-1(Hazardous Substances Data)

Usage

General Description

Ethanone, 1-[2-(1H-pyrazol-1-yl)phenyl]- is a chemical compound that is synthesized by combining ethanone with 1-[2-(1H-pyrazol-1-yl)phenyl]. It is primarily used in research and scientific studies as a reagent or intermediate in the synthesis of other compounds. This chemical may have potential applications in pharmaceutical research, particularly in the development of new drugs targeting specific receptors or biological pathways. Further studies are needed to understand the exact properties and potential uses of this chemical compound.

Upstream product

• 288-13-1 NH-pyrazole 
• 445-27-2 2'-Fluoroacetophenone 
• 1126-00-7 1-phenylpyrazole 
• 64-19-7 acetic acid 
• 87488-84-4 1-(2-bromophenyl)pyrazole 
• 78191-00-1 N-Methoxy-N-methylacetamide 
• 75-36-5 acetyl chloride 

Relevant articles and documents

Monodisperse CuPd alloy nanoparticles as efficient and reusable catalyst for the C (sp2)–H bond activation

Metal-catalyzed selective activation of C–H bonds is very important for the construction of a variety of biologically active molecules. Supported alloy nanoparticles are of great interest in various catalytic applications due to the synergistic effects between different metals. Here, well-dispersed CuPd alloy nanoparticles supported on reduced graphene oxide (rGO) were synthesized and found to be highly efficient and recyclable catalyst for the chelation-assisted C (sp2)–H bond activation. Aromatic ketones or esters were synthesized via the cross-dehydrogenative coupling (CDC) reaction between 2-arylpyridines and alcohols or acids. Moreover, the catalyst was recovered and used for five times without significantly losing activity.

Catalytic, Directed C-C Bond Functionalization of Styrenes

A method for catalytic conversion of C(aryl)-C(alkenyl) bonds in styrene derivatives to new C-C bonds is developed. In the presence of a rhodium catalyst, the alkenyl groups of styrenes bearing a pyrazolyl directing group were efficiently converted to other carbon substituents upon reacting with various alkenes including styrenes, aliphatic alkenes, and allyl alcohols. It is also indicated that the C-C bond cleavage proceeded via a hydrometalation/β-carbon elimination pathway.

Ruthenium-catalyzed C-H functionalization of arylpyrazoles: Regioselective acylation with acid chlorides

A ruthenium-catalyzed C-H acylation of arylpyrazoles with a variety of acyl chlorides is described. The acylation reaction exhibits good regioselectivity and both aromatic and aliphatic acyl chlorides can be effectively coupled to the arylpyrazoles at the