60712-44-9

Basic information

• Product Name: 3,4,6-trichloroguaiacol
• Synonyms: 3,4,6-trichloroguaiacol
• CAS NO: 60712-44-9
• Molecular Formula: C₇H₅Cl₃O₂
• Molecular Weight: 227.47
• Mol File: 60712-44-9.mol

Chemical Properties

• Boiling Point: 283.5°C at 760 mmHg
• Flash Point: 125.3°C
• Appearance: /
• Density: 1.539g/cm³
• Vapor Pressure: 0.00183mmHg at 25°C
• Refractive Index: 1.584
• CAS DataBase Reference: 3,4,6-trichloroguaiacol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4,6-trichloroguaiacol(60712-44-9)
• EPA Substance Registry System: 3,4,6-trichloroguaiacol(60712-44-9)

Safety Data

• Hazardous Substances Data: 60712-44-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H5Cl3O2/c1-12-7-5(10)3(8)2-4(9)6(7)11/h2,11H,1H3

Upstream product

• 77102-94-4 3,4-Dichloro-2-methoxyphenol 
• 90-05-1 2-methoxy-phenol 
• 77102-95-5 5,6-Dichloro-2-methoxyphenol 
• 85430-14-4 5,6-dichloroguaiacol acetate 
• 85430-08-6 6-chloroguaiacol acetate 
• 72403-03-3 2-methoxy-6-chlorophenol 
• 3978-67-4 3,4-dichloro-1,2-benzenediol 
• 77102-93-3 3,6-Dichloro-2-methoxyphenol 

Relevant articles and documents

Mass Spectra of Chlorinated Aromatics Formed in Pulp Bleaching. 2-Chlorinated Guaiacols

The fragmentation of chlorinated guaiacols (2-methoxyphenols) on electron impact has been studied.The most common fragmentation processes are interpreted and in some cases the small differences between spectra of positional isomers are explained.In addition to the well-known alkyl-oxygen fission (loss of methyl radical), metastable ion studies and deuterium labelling have indicated several new fragmentation pathways.The most characteristic are the formation of + and +. ions.In general, however, the spectra of positional isomers are shown to be very similar.

Isomer specific syntheses of chlorinated catechols and guaiacols relevant to pulp bleaching

A variety of chlorinated catechols and guaiacols relevant to pulp bleaching were synthesized by employing fundamental differences in the acidities of phenolic hydroxyl groups in chlorinated catechols, and directive effects in guaiacols.