2808-86-8 Usage
Description
2,3,4,5-Tetrachloropyridine is a heterocyclic aromatic organic compound belonging to the pyridine and pyridine derivatives family. It is characterized by the molecular formula C5HCl4N and exhibits a colorless or yellowish liquid appearance. This highly toxic and potentially carcinogenic compound can cause irritation upon skin contact, inhalation, or ingestion. Primarily used for research purposes, 2,3,4,5-tetrachloropyridine is not a common component of human or environmental exposure. Safe handling and proper storage are essential to prevent potential health hazards. The long-term effects and interactions of this chemical with other substances are not well understood due to limited research in this area.
Uses
Used in Research Applications:
2,3,4,5-Tetrachloropyridine is used as a research chemical for [application reason]. Due to its highly toxic and potentially carcinogenic nature, it is primarily utilized in controlled laboratory settings for specific research purposes. 2,3,4,5-tetrachloropyridine's properties and reactions can provide valuable insights into various chemical and biological processes.
Used in Chemical Synthesis:
In the chemical synthesis industry, 2,3,4,5-tetrachloropyridine is used as an intermediate or reactant for the production of other chemicals. Its unique structure and reactivity make it a valuable component in the synthesis of various compounds with specific applications in different industries.
Used in Pharmaceutical Research:
2,3,4,5-Tetrachloropyridine is employed in pharmaceutical research as a potential candidate for the development of new drugs or drug delivery systems. Its unique chemical properties may offer novel therapeutic approaches or enhance the efficacy of existing treatments.
Used in Agrochemical Development:
In the agrochemical industry, 2,3,4,5-tetrachloropyridine is used as a starting material or intermediate in the development of new pesticides or herbicides. Its chemical properties may contribute to the creation of more effective and targeted agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 2808-86-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2808-86:
(6*2)+(5*8)+(4*0)+(3*8)+(2*8)+(1*6)=98
98 % 10 = 8
So 2808-86-8 is a valid CAS Registry Number.
InChI:InChI=1/C5HCl4N/c6-2-1-10-5(9)4(8)3(2)7/h1H
2808-86-8Relevant articles and documents
Resourceful treatment method of picloram solid residues
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Paragraph 0059-0064, (2020/11/23)
The invention relates to a picloram solid residue resourceful treatment method which comprises the following steps: a) carrying out decarboxylation reaction on picloram solid residues, performing filtering, taking filtrate, and separating out solid; b) sequentially carrying out diazotization and chlorination reaction on the solid obtained in the step a), separating out the solid, performing filtering, taking a filter cake, and performing separating to obtain 2, 3, 4, 5-tetrachloropyridine; c) subjecting the 2, 3, 4, 5-tetrachloropyridine obtained in the step b) to a dechlorination reaction soas to obtain 2, 3, 5-trichloropyridine and/or 2, 5-dichloropyridine. According to the resourceful treatment method provided by the invention, the picloram solid residues can be converted into 2, 3, 5-trichloropyridine products with good market demand prospects and relatively high economic values, and further efficient utilization of the picloram solid residues is realized.
DESTRUCTIVE CHLORINATION OF 3,4,5-TRICHLORO-2-(TRICHLOROMETHYL)PYRIDINE
Emel'yanov, V. I.,Stul', B. Ya.,Korolev, B. M.
, p. 1168 - 1171 (2007/10/02)
The extensive destructive chlorination of 3,4,5-trichloro-2-(trichloromethyl)pyridine proceeds by both thermal (160-245 deg C) and photochemical pathways.Perchloropyridine, perchloropicoline, and carbon tetrachloride are formed.The chlorinated derivatives of pyridine are formed by the loss of the CCl3 group with its subsequent replacement by a chlorine atom.
