37665-07-9

Upstream product

• 10469-02-0 3,4,5,6-tetrachloro-2-methylpyridine 

Downstream Products

• 135781-99-6 2-benzyltetrachloropyridine 
• 135782-10-4 <4-(allyloxycarbonyl)tetrachlorophenyl>(pentachlorophenyl)(tetrachloro-2-pyridyl)methyl radical 
• 135782-07-9 <4-(allyloxycarbnyl)tetrachlorophenyl>(pentachlorophenyl)(tetrachloro-2-pyridyl)methane 
• 135782-09-1 (pentachlorophenyl)(tetrachloro-2-pyridyl)methyl radical 
• 135782-08-0 (4-carboxytetrachlorophenyl)(pentachlorophenyl)(tetrachloro-2-pyridyl)methyl radical 
• 135782-06-8 (pentachlorophenyl)(tetrachloro-2-pyridyl)methane 
• 135782-05-7 4-carboxytetrachlorophenyl(pentachlorophenyl)(tetrachloro-2-pyridyl)methane 
• 135782-03-5 (pentachlorophenyl)<2,3,5,6-tetrachloro-4-(dichloromethyl)phenyl>(tetrachloro-2-pyridyl)methane 
• 135782-04-6 (pentachlorophenyl)(tetrachloro-4-formylphenyl)(tetrachloro-2-pyridyl)methane 
• 135782-02-4 (pentachlorophenyl)(tetrachloro-4-methylphenyl)(tetrachloro-2-pyridyl)methane 
• 135781-98-5 phenyl(tetrachloro-2-pyridyl)(p-tolyl)methanol 
• 135782-01-3 phenyl(tetrachloro-2-pyridyl)(p-tolyl)methane 
• 135782-00-2 tetrachloro-2-(α,α-dichlorobenzyl)pyridine 
• 38373-64-7 2-benzoyltetrachloropyridine 

Relevant academic research and scientific papers

Monofunctionalized Tridecachlorodiphenyl(2-pyridyl)methyl Radicals. Synthesis and Spectral Analysis

Highly chlorinated diphenyl(2-pyridyl)methyl radicals and their α-H precursors with a carboxy, chlorocarbonyl, or allyloxycarbonyl substituent in the 4-position of one phenyl ring have been synthesized.All of them are stable red solids, completely dissociated (magnetic susceptibility), decomposing when melting (200-240 deg C).Their ESR, UV-Vis and IR spectra are given.