141632-21-5

Basic information

• Product Name: 3-(2-Fluorophenyl)cyclohexanone
• Synonyms: 3-(2-Fluorophenyl)cyclohexanone
• CAS NO: 141632-21-5
• Molecular Formula: C12H13FO
• Molecular Weight: 192.2294232
• Mol File: 141632-21-5.mol
• Article Data: 13

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-(2-Fluorophenyl)cyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-Fluorophenyl)cyclohexanone(141632-21-5)
• EPA Substance Registry System: 3-(2-Fluorophenyl)cyclohexanone(141632-21-5)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 141632-21-5(Hazardous Substances Data)

Usage

General Description

3-(2-Fluorophenyl)cyclohexanone, also known as 2'-fluoro-3'-phenylcyclohexanone, is a chemical compound with the molecular formula C13H15FO. It is a ketone derivative with a cyclohexane ring and a fluorophenyl group attached to it. This chemical is often used as an intermediate in the synthesis of pharmaceuticals and organic compounds. It can also be used as a building block in the development of new compounds for medical research and drug discovery. Additionally, 3-(2-Fluorophenyl)cyclohexanone may have potential applications in the field of organic chemistry for the creation of new materials and substances. 3-(2-Fluorophenyl)cyclohexanone is of interest to scientists and researchers due to its unique structure and potential for use in various chemical reactions and applications.

Upstream product

• 930-68-7 cyclohexenone 
• 1993-03-9 o-fluorophenylboronic acid 

Relevant articles and documents

The synthesis method of one-carbon ring expansion of cycloketone dericatives from β-selenyl cycloketone dericatives

The present invention relates to a method for preparing a cyclic ketone derivative with an increased carbon number by performing a ring expansion reaction of a β-selenyl cyclic ketone derivative. The present invention was first developed by performing the

Electrochemical Radical Selenylation/1,2-Carbon Migration and Dowd-Beckwith-Type Ring-Expansion Sequences of Alkenylcyclobutanols

Electrochemical oxidative radical selenylation/1,2-carbon migration and Dowd-Beckwith-type ring-expansion sequences of alkenylcyclobutanols were developed in this study. This approach is environmentally benign and uses shelf-stable diselenides as selenium

Sulfoxide-alkene hybrids: A new class of chiral ligands for the Hayashi-Miyaura reaction

Sulfoxide-alkene hybrids are introduced as a new class of chiral heterodentate ligands for the Hayashi-Miyaura reaction. The synthesis of these ligands was achieved without the use of protecting groups. A chiral resolution was performed via simple column-chromatographic separation of the diastereomeric ligands. Both diastereomers proved to be excellent ligands in Rh-catalyzed 1,4-addition reactions, furnishing chiral products with high enantioselectivities and, remarkably, opposite stereoconfigurations.