2136-96-1

Upstream product

• 634-90-2 1,2,3,5-tetrachlorobenzene 
• 67-66-3 chloroform 
• 108-38-3 m-xylene 
• 877-09-8 2,4,5,6-tetrachloro-1,3-dimethylbenzene 

Downstream Products

• 40860-93-3 tetrachloro-isophthalaldehyde 
• 33240-61-8 αH-Pentadecachlorotriphenylmethane 
• 131380-97-7 2,4,5,6-tetrachloro-α,α,α',α'-tetrakis(pentachlorophenyl)-m-xylene 
• 127316-84-1 2,4,5,6-tetrachloro-α,α,α',α'-tetrakis(pentachlorophenyl)-m-xylylene biradical 
• 131380-98-8 2,4,5,6-tetrachloro-α,α,α',α'-tetrakis(pentachlorophenyl)-m-xylyl radical 
• 192511-39-0 2,4,5,6-Tetrachloro-isophthalonitrile N,N'-dioxide 
• 192511-41-4 2,4,5,6-Tetrachloro-benzene-1,3-dicarbaldehyde dioxime 

Relevant academic research and scientific papers

Synthesis of tetrachloroisophthalic and -terephthalic aldehydes and stable bis(nitrile oxides) based on them

A new route for the synthesis of 2,4,5,6-tetrachloroisophthalic and 2,3,5,6-tetrachloro-terephthalic aldehydes from the corresponding tetrachlorobenzenes was developed. The method involves dichloromethylation of the initial compounds with chloroform in th

Stable polyradicals with high-spin ground states. 1, synthesis, separation, and magnetic characterization of the stereoisomers of 2,4,5,6-tetrachloro-α, α, α', α'-tetrakis(pentachlorophenyl)-m-xylylene biradical

Biradical 3 and its corresponding monoradical 6 have been synthesized and isolated as stable solids at ambient conditions. Biradical 3 exists in three stereoisomeric forms due to restricted correlated rotation of the aryl groups. It has obtained as a 60:4