52112-24-0

Basic information

• Product Name: Benzene, 1-fluoro-3-(1-propynyl)- (9CI)
• Synonyms: Benzene, 1-fluoro-3-(1-propynyl)- (9CI);Benzene, 1-fluoro-3-(1-propyn-1-yl)-
• CAS NO: 52112-24-0
• Molecular Formula: C₉H₇F
• Molecular Weight: 134.1502832
• Mol File: 52112-24-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzene, 1-fluoro-3-(1-propynyl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-fluoro-3-(1-propynyl)- (9CI)(52112-24-0)
• EPA Substance Registry System: Benzene, 1-fluoro-3-(1-propynyl)- (9CI)(52112-24-0)

Safety Data

• Hazardous Substances Data: 52112-24-0(Hazardous Substances Data)

Usage

General Description

Benzene, 1-fluoro-3-(1-propynyl)- (9CI) is a chemical compound with the molecular formula C9H7F. It is a fluorinated derivative of benzene with a propynyl side chain. Benzene, 1-fluoro-3-(1-propynyl)- (9CI) is primarily used in the manufacturing of pharmaceuticals, agrochemicals, and dyes. It is also used in the production of polymers and as a solvent. In terms of its properties, benzene, 1-fluoro-3-(1-propynyl)- (9CI) is a colorless liquid with a strong aromatic odor. It is flammable and should be handled with caution due to its potential health and environmental hazards.

Upstream product

• 590-93-2 2-Butynoic acid 
• 1073-06-9 3-fluorobromobenzene 
• 75-20-7 calcium carbide 
• 2561-17-3 1-ethynyl-3-fluoro-benzene 
• 74-88-4 methyl iodide 
• 705-83-9 3-(m-fluorophenyl)-propiolic acid 
• 917-54-4 methyllithium 

Downstream Products

• 38340-11-3 1-fluoro-3-(1-propen-1-yl)benzene 

Relevant articles and documents

Enantioselective Resolution Copolymerization of Racemic 2,3-Disubstituted cis-Epoxides with CO2 Mediated by Binuclear Cobalt(III) Catalyst?

Enantioselective resolution copolymerization of racemic internal epoxides with carbon dioxide (CO2) is a challenging issue because of their poor reactivity and complicated regio/stereoselectivity. Herein, we describe the first enantioselective

Rh-Catalyzed Asymmetric Hydrogenation of α,β- and β,β-Disubstituted Unsaturated Boronate Esters

A highly enantioselective hydrogenation of α,β-unsaturated boronate esters catalyzed by Rh-(S)-DTBM-Segphos complex has been developed. Both (Z)-α,β- and β,β-disubstituted substrates can be successfully hydrogenated to afford chiral boronates with excellent enantioselectivities, up to 98 % ee. Furthermore, the obtained chiral boronate esters, as important versatile synthetic intermediates are successfully transformed to the corresponding chiral alcohols, amines and other important derivatives with maintained enantioselectivities.