116272-42-5

Basic information

• Product Name: 5-CHLORO-2-FLUOROIODOBENZENE
• Synonyms: 4-CHLORO-1-FLUORO-2-IODOBENZENE;5-CHLORO-2-FLUOROIODOBENZENE;5-Chloro-2-fluoroiodobenzene97%
• CAS NO: 116272-42-5
• Molecular Formula: C₆H₃ClFI
• Molecular Weight: 256.44
• Mol File: 116272-42-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 226.3 °C at 760 mmHg
• Flash Point: 90.7 °C
• Appearance: /
• Density: 2.008 g/cm³
• Vapor Pressure: 0.124mmHg at 25°C
• Refractive Index: 1.606
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: 5-CHLORO-2-FLUOROIODOBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-CHLORO-2-FLUOROIODOBENZENE(116272-42-5)
• EPA Substance Registry System: 5-CHLORO-2-FLUOROIODOBENZENE(116272-42-5)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 36/37/38-36-22
• Safety Statements: 26-36
• Hazardous Substances Data: 116272-42-5(Hazardous Substances Data)

Usage

General Description

5-Chloro-2-Fluoroiodobenzene is a chemical compound categorized under the class of organofluorides and organochlorides. It combines elements of chlorine, fluorine, iodine, and benzene in its structure, making it relevant in a variety of chemical reactions and laboratory processes. 5-CHLORO-2-FLUOROIODOBENZENE is used predominantly as a reactant in the synthesis of other chemical compounds. Moreover, its chemical properties include a molecular weight of 290.37 g/mol and a molecular formula of C6H3ClFI. It is generally a solid mass or crystals with a sharp, strong odor, and it must be handled with caution due to its potential reactivity and hazards associated with its elements.

InChI:InChI=1/C6H3ClFI/c7-4-1-2-5(8)6(9)3-4/h1-3H

Upstream product

• 63069-48-7 p-chloro-o-iodoaniline 

Relevant articles and documents

Synthesis of 2,4-dihalogenofluorobenzenes and their antimicrobial and antifungal activity studies

The aim of this study was to synthesize and identify 2,4- dihalogenofluorobenzene (or trihalogenobenzene) derivatives by spectroscopic means, 1H-NMR and 19F-NMR. The 2,4-dihalofluorobenzene derivatives considered were 2,4-dichlorofluorobenzene (1), 2-bromo-4- chlorofluorobenzene (2), 2-iodo-4-chlorofluorobenzene(3), 2,5- dichlorofluorobenzene (4), 2-bromo-5-chlorofluorobenzene (5), 2-iodo-5-chlorofluorobenzene (6). The in vitro antibacterial and antifungal activities of trihalogenobenzene derivatives were studied against the bacteria Staphylococcus aureus ATCC 25923 Gram(+), Bacillus cereus ATCC 6633 Gram(+), Micrococcus flavus (clinical isolate) Gram(+), Morgenella morganii (clinical isolate) Gram(-), Escherichia coli ATCC 27853 Gram(-) and fungus Candida albicans (clinical isolate), obtained from the biology departments of the Pamukkale and Gazi Universities. The antibacterial and antifungal activities were measured by minimum inhibition concentration (MIC) method and the disc-diffusion method used to measure zone diameter against Gram-positive and Gram-negative bacteria and fungi. All these bacteria and fungi were studied against antibiotics to compare the zone diameters with the results from our treatments. Birkhaeuser 2007.