400-01-1

Basic information

• Product Name: 2,4,5-TriMethylfluorobenzene
• Synonyms: 2,4,5-TriMethylfluorobenzene
• CAS NO: 400-01-1
• Molecular Formula: C₉H₁₁F
• Molecular Weight: 138.1820432
• Mol File: 400-01-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 175.4±9.0 °C(Predicted)
• Appearance: /
• Density: 0.969±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2,4,5-TriMethylfluorobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,5-TriMethylfluorobenzene(400-01-1)
• EPA Substance Registry System: 2,4,5-TriMethylfluorobenzene(400-01-1)

Safety Data

• Hazardous Substances Data: 400-01-1(Hazardous Substances Data)

Usage

General Description

2,4,5-Trimethylfluorobenzene is a chemical compound with the molecular formula C9H11F. It is a colorless liquid with a pleasant, aromatic odor and is commonly used as a solvent in various industrial applications. 2,4,5-Trimethylfluorobenzene is highly flammable and should be handled with care. 2,4,5-Trimethylfluorobenzene is also classified as a hazardous material and is subject to strict regulations regarding its production, storage, and transportation. It is important to use proper safety measures when working with this chemical to avoid potential health risks and environmental pollution.

Upstream product

• 137-17-7 2,4,5-trimethylaniline 
• 95-93-2 1,2,4,5-tetramethylbenzene 
• 95-63-6 1,2,4-Trimethylbenzene 

Relevant articles and documents

Metal-Catalyzed Carbon-Fluorine Bond Formation

One aspect of the invention relates to a metal-catalyzed conversion of aryl halides and sulfonates to the corresponding aryl fluorides. Another aspect of the invention relates to a metal-catalyzed conversion of heteroaryl halides and sulfonates to the corresponding heteroaryl fluorides. Another aspect of the invention relates to a metal-catalyzed conversion of vinyl halides and sulfonates to the corresponding vinyl fluorides. In certain embodiments, simple fluoride sources, such as AgF and CsF, are used. In certain embodiments, the transformations tolerate a wide range of functional groups, allowing for introduction of fluorine atoms into highly functionalized organic molecules.

Effect of Catalyst on the Fluorination of Methyl-Substituted Benzenes with Xenon Difluoride

The course of acid-catalyzed liquid-phase fluorination of methyl-substituted benzene derivatives with xenon difluoride depends strongly on the structure and concentration of the substrate, its molar ratio to xenon difuoride, and the catalyst.HF-catalyzed