3849-01-2

Basic information

• Product Name: 1,3,5-Tris-chloroMethyl-2,4,6-triMethyl-benzene
• Synonyms: 1,3,5-Tris-chloroMethyl-2,4,6-triMethyl-benzene;2,4,6-Tris(chloroMethyl)Mesitylene;1,3,5-Trimethyl-2,4,6-tris(chloromethyl)benzene;NSC 156141;Tris(chloromethyl)mesitylene
• CAS NO: 3849-01-2
• Molecular Formula: C₁₂H₁₅Cl₃
• Molecular Weight: 237.55334
• EINECS: -0
• Mol File: 3849-01-2.mol
• Article Data: 8

Chemical Properties

• Melting Point: 170-171℃
• Boiling Point: 370.2°Cat760mmHg
• Flash Point: 258°C
• Appearance: White/Powder
• Density: 1.199
• Vapor Pressure: 2.4E-05mmHg at 25°C
• Refractive Index: 1.545
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 1,3,5-Tris-chloroMethyl-2,4,6-triMethyl-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Tris-chloroMethyl-2,4,6-triMethyl-benzene(3849-01-2)
• EPA Substance Registry System: 1,3,5-Tris-chloroMethyl-2,4,6-triMethyl-benzene(3849-01-2)

Safety Data

• HazardClass: 8
• Hazardous Substances Data: 3849-01-2(Hazardous Substances Data)

Usage

General Description

1,3,5-Tris-chloroMethyl-2,4,6-triMethyl-benzene is a chemical compound that is commonly used as a pesticide and fungicide. It is a derivative of benzene and contains three chlorine atoms and three methyl groups. It is a white solid with a strong odor and is highly toxic to humans and the environment. It is used to control pests and disease in agriculture, as well as in the treatment of wood and textiles. However, it has been banned or restricted in several countries due to its hazardous effects on human health and the environment, including its potential to cause cancer and disrupt hormone systems.

InChI:InChI=1/C12H15Cl3/c1-7-10(4-13)8(2)12(6-15)9(3)11(7)5-14/h4-6H2,1-3H3

Upstream product

• 107-30-2 chloromethyl methyl ether 
• 108-67-8 1,3,5-trimethyl-benzene 
• 50-00-0 formaldehyd 
• 20145-50-0 pentamethylbenzyl methyl ether 
• 87-85-4 Hexamethylbenzene 

Downstream Products

• 1189554-32-2 1,3,5-tris(benzyloxymethyl)-2,4,6-tris(phthalimidomethyl)-benzene 
• 1709-70-2 1,3,5-trimethyl-2,4,6-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)benzene 
• 71715-84-9 2,4,6-tris(o-aminophenylthiomethyl)mesitylene 
• 155340-26-4 1,3,5--2,4,6-trimethylbenzene 
• 410074-21-4 1,3,5-tris(bromomethyl)-2,4,6-tris(chloromethyl)benzene 
• 70477-56-4 1,3,5-tris(thiocyanatomethyl)mesitylene 
• 1974-32-9 1,3,5-Tris(acetoxymethyl)-2,4,6-trimethylbenzene 
• 3095-73-6 1,2,3,4,5,6-hexa(bromomethyl)benzene 
• 66628-58-8 2-Chloromethyl-7-methyl-tricyclo[6.2.0.0^3,6]deca-1⁽⁸⁾,2,6-triene 
• 3227-93-8 hexaradialene 
• 71190-18-6 C₃₆H₃₆O₉ 
• 172606-27-8 1,3,5-tris(3,5-dimethylpyrazole-1-yl-methyl)-2,4,6-trimethylbenzene 
• 69020-18-4 1,3,5-Trimethyl-2,4,6-tris-trimethylsilanylmethyl-benzene 

Relevant articles and documents

Tripodal ligand containing 3, 5-dimethylpyrazole, synthesis method of tripodal ligand and application

The invention relates to a tripodal ligand containing 3, 5-dimethylpyrazole, a synthesis method of the tripodal ligand and an application. The technical scheme includes that anhydrous ZnCl2, paraformaldehyde, concentrated hydrochloric acid and 1, 3, 5-tri

Insights into the formation of chiral second sphere coordination complexes with aromatic tris amines: combined single crystal X-ray crystallography and molecular modeling analyses

A family of isostructural, chiral supramolecular networks have been obtained in the solid state by exploiting second sphere coordination interactions in the self-assembly of achiral tris amines L1 and L2 with tetrahalometallate and halide ions. Quantum-Mechanical (QM) calculations specific for solid phases provided additional insights into the intramolecular and packing interactions which determine chirality, pointing to a direct effect of the methyl groups of the central benzene ring.

Ion-pair binding: Is binding both binding better?

It is often tempting to explain chemical phenomena on the basis of intuitive principles, but this practice can frequently lead to biased analysis of data and incorrect conclusions. One such intuitive principle is brought into play in the binding of salts