877-11-2

Usage

Uses

Used in Environmental Research:
2,3,4,5,6-PENTACHLOROTOLUENE is used as a predictive chemical in environmental studies for assessing the survival of aquatic organisms, such as daphnids, after in situ exposure to complex mixtures. Its application in this field helps researchers understand the potential impact of environmental contaminants on aquatic life.
Used in Chemical Analysis:
Due to its unique properties, 2,3,4,5,6-PENTACHLOROTOLUENE can be employed as a reference compound in chemical analysis and toxicological studies. This helps in the development of methods to detect and measure the presence of toxic substances in various environmental samples.

InChI:InChI=1/C7H3Cl5/c1-2-3(8)5(10)7(12)6(11)4(2)9/h1H3

Upstream product

• 14152-24-0 1,2,3,4,5,6-Hexachlorcycloheptan 
• 108-88-3 toluene 
• 42413-03-6 3-chloro-4-methylbenzenesulfonyl chloride 
• 10025-91-9 antimony(III) chloride 
• 7782-50-5 chlorine 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 135782-01-3 phenyl(tetrachloro-2-pyridyl)(p-tolyl)methane 
• 7359-72-0 2,3,4-trichlorotoluene 
• 6639-30-1 2,4,5-trichlorotoluene 
• 99-87-6 4-methylisopropylbenzene 
• 530-45-0 1,1-di(4-methylphenyl)ethane 

Downstream Products

• 56680-65-0 2,3,5,6-tetrachloro-4-methylphenol 
• 52221-93-9 2,3,4,5,6-Pentachlor-N,N-dimethylbenzylamin 
• 2037-26-5 ⁽²⁾H₈-toluene 
• 39569-02-3 2-chloro-3-pentachlorophenylpropanoic acid 
• 4960-52-5 2,3,4,5,6-Pentachlor-benzylamin 
• 39569-00-1 pentachlorophenyl-phenyl-methane 
• 18412-83-4 acetic acid-(2,3,4,5,6-pentachloro-benzyl ester) 
• 29082-75-5 β,β,2,3,4,5,6-heptachlorostyrene 
• 2136-95-0 pentachloro-α,α-dichlorotoluene 
• 34037-69-9 C₇H₃Cl₅O₇S₂ 
• 34037-70-2 C₇H₃Cl₅O₁₄S₄ 
• 16022-69-8 2,3,4,5,6-pentachlorobenzylalcohol 
• 19635-52-0 2,3,4,5,6-pentachlorobenzaldehyde 
• 36593-26-7 α-bromo-2,3,4,5,6-pentachlorotoluene 

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.

DESTRUCTIVE CHLORINATION OF ALKYLBENZENES ON HETEROGENEOUS CATALYSTS.

A study was made of the destructive chlorination of alkylbenzenes in the vapor phase on metal oxides and metal chlorides. This work shows that 380-400 degree C, 11-12 sec contact time, 0. 3-0. 8 mass % MoO//3 on alumina, 7-10% stoichiometric excess of chlorine, and 1:9 toluene/chlorine mole ratio were optimal for the chlorination of toluene to give C//6Cl//6 and CCl//4. The optimal conditions for the preparation of pentachlorobenzyl chloride were 295-320 degree C, 18-22 sec contact time, 1:6 toluene/chlorine mole ratio, and 4-8. 5 mass % MgCl//2 on KSK silica gel. The optimal yields of CCl//4 and C//6Cl//6 were 97. 4-98. 2 and 93. 8-96. 3 mole %, respectively, with 91-93 mole % conversion of chlorine.

Chlorination process

Process for nuclear chlorination of non-phenolic aromatic compounds, said process comprising contacting and reacting a non-phenolic aromatic compound having a net Hammett ? value of about -0.1 to about 2.0 with chlorine monoxide in the presence of at least one-half an equivalent amount, based on the chlorine monoxide, of an acid having a pKa no greater than that of trichloroacetic acid, provided, however, when the net Hammett ? value is about 0.7 to about 2.0, the acid has a pKa no greater than that of trifluoroacetic acid.