1,2,4-trichlorobenzene

Base Information Edit

Chemical Name:1,2,4-trichlorobenzene
CAS No.:63697-18-7
Molecular Formula:C₆H₃Cl₃
Molecular Weight:181.449
Hs Code.:
Mol file:63697-18-7.mol

Synonyms:1,2,4-Trichlorobenzeneradical anion

Suppliers and Price of 1,2,4-trichlorobenzene

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 6 raw suppliers

Chemical Property of 1,2,4-trichlorobenzene Edit

Chemical Property:

Melting Point:17ºC
Boiling Point:211.4 °C at 760 mmHg
Flash Point:126.7 °C
Density:1.448 g/cm³
Water Solubility.:Insoluble in water, slightly soluble in alcohol, soluble in ether, benzene and carbon bisulfide

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1,2,4-trichlorobenzene

There total 157 articles about 1,2,4-trichlorobenzene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 73.0%

: 95-94-3
1,2,4,5-tetrachlorobenzene

: 106-46-7,84348-21-0
para-dichlorobenzene

: 108-90-7
chlorobenzene

: 95-50-1
1,2-dichloro-benzene

: 541-73-1
1,3-Dichlorobenzene

: 120-82-1,63697-18-7
1,2,4-Trichlorobenzene

: 71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1
benzene

Guidance literature:: With potassium hydroxide; hydrogen; palladium on activated charcoal; In water; at 50 ℃; for 0.5h; Product distribution; Aliquat 336 and other phase-transfer catalysts, different multiphase systems, different time and solvents;
DOI:10.1021/jo00071a041

Reference yield: 9.0%

: 95-94-3
1,2,4,5-tetrachlorobenzene

: 106-46-7,84348-21-0
para-dichlorobenzene

: 95-50-1
1,2-dichloro-benzene

: 541-73-1
1,3-Dichlorobenzene

: 120-82-1,63697-18-7
1,2,4-Trichlorobenzene

Guidance literature:: With carbon dioxide; tetrabutylammomium bromide; In N,N-dimethyl-formamide; at -5 - 0 ℃; Further byproducts given; Electrochemical reaction;
DOI:10.1135/cccc20000862

Reference yield:

: 88-06-2,67471-29-8
2,4,6-Trichlorophenol

: 87-86-5,67471-28-7
Pentachlorophenol

: 108-70-3,63697-19-8
1,3,5-trichlorobenzene

: 120-82-1,63697-18-7
1,2,4-Trichlorobenzene

: 87-61-6
1,2,3-trichlorobenzene

Guidance literature:: With oxygen; fly ash; at 400 ℃; Further byproducts given. Title compound not separated from byproducts; Formation of xenobiotics;
DOI:10.1016/S0045-6535(00)00244-7