5006-38-2

Basic information

• Product Name: 2,4,5-TRIFLUOROANISOLE
• Synonyms: 2,4,5-TRIFLUOROANISOLE;TRIFLUOROANISOLES
• CAS NO: 5006-38-2
• Molecular Formula: C₇H₅F₃O
• Molecular Weight: 162.11
• Mol File: 5006-38-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 152.8°C at 760 mmHg
• Flash Point: 58.3°C
• Appearance: /
• Density: 1.285g/cm³
• Vapor Pressure: 4.39mmHg at 25°C
• Refractive Index: 1.435
• CAS DataBase Reference: 2,4,5-TRIFLUOROANISOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,5-TRIFLUOROANISOLE(5006-38-2)
• EPA Substance Registry System: 2,4,5-TRIFLUOROANISOLE(5006-38-2)

Safety Data

• RIDADR: 1325
• HazardClass: 4.1
• PackingGroup: III
• Hazardous Substances Data: 5006-38-2(Hazardous Substances Data)

Usage

General Description

2,4,5-Trifluoroanisole is a chemical compound with the molecular formula C7H5F3O. It is a colorless liquid with a sweet, aromatic odor. 2,4,5-Trifluoroanisole is commonly used as a flavoring agent and in the production of pharmaceuticals and agrochemicals. It is also used as an intermediate in organic synthesis reactions. The compound is considered to be relatively stable and has low water solubility. However, it has been identified as a potential environmental contaminant and may be harmful if swallowed, inhaled, or absorbed through the skin. Therefore, proper safety precautions should be taken when handling 2,4,5-Trifluoroanisole.

InChI:InChI=1/C7H5F3O/c1-11-7-3-5(9)4(8)2-6(7)10/h2-3H,1H3

Upstream product

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Relevant articles and documents

Fluorine analogs of dicamba and tricamba herbicides; Synthesis and their pesticidal activity

Fluorine analogs of the dicamba and tricamba herbicides were synthesized. Their herbicide activities were compared with the activities of the pattern herbicides dicamba and tricamba.

Mechanisms for Reactions of Halogenated Compounds. Part 3. Variation in Activating Influence of Halogen Substituents in Nucleophilic Aromatic Substitution

Rate constants are reported for reactions of polyhalogeno-pyridines and -benzenes with sodium methoxide in methanol.Relative activating effects of individual fluorine and chlorine atoms at positions ortho, meta, and para to the reaction site are determined and compared with orders determined from reactions involving ammonia in aqueous dioxan.The results are remarkably similar.Additional support is provided for earlier explanations of the activating effects of ortho-fluorine and -chlorine.Activation parameters, determined for reactions of polyhalogenepyridines with ammonia in aqueous dioxan, clearly demonstrate that differences in reactivity along the series arise mainly from changes in activation energy.